PubChem | Glycans

Symbol Nomenclature for Glycans (SNFG)

Created: October 15, 2015; Last updated: February 26, 2024

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Standardization in drawing glycan structures is essential for efficient communication. The tools and methodology illustrated here have become widely accepted by the scientific community. Use of these symbols to represent glycans is now strongly recommended for all scientific manuscripts and other publications. The following are pages with additional information about the Symbol Nomenclature For Glycans (SNFG):

History of the SNFG

The SNFG Discussion Group

Organizations and Publications Adopting SNFG

Software tools supporting the SNFG

Primary citation for the SNFG:

• Symbol Nomenclature for Graphical Representation of Glycans, Glycobiology 25: 1323-1324, 2015. Citation link (PMID 26543186).
• Updates to the Symbol Nomenclature for Glycans guidelines, Glycobiology 29:620-624, 2019. Citation link (PMID 31184695).

Other citations:

• Cataloging natural sialic acids and other nonulosonic acids (NulOs), and their representation using the Symbol Nomenclature for Glycans, Glycobiology 33: 99-103, 2023. Citation link (PMID 36648443; NCBI page describing natural sialic acids and Nonulosonic acids).

Page Content

• SNFG rendering programs
• Symbol Nomenclature
• Examples of Glycan Symbol Nomenclature
• CMYK and RGB color assignments
• Substituent list and chemical structures
• Monosaccharide abbreviations and names
• Updates to SNFG versions
• License

SNFG rendering programs ☝

1. 3D-Symbol Nomenclature for Glycans (3D-SNFG): Create 3D atomic models of glycans
   Direct weblink | Citation link.
2. DrawGlycan SNFG: Convert IUPAC input strings to sketches of glycans and glycopeptides
   Direct weblink | App download | Citation link.
3. GlycanBuilder2-SNFG: GlycanBuilder updated to handle SNFG
   App download | Citation link.
4. CSDB glycan editor: Creates SNFG and 3D-models of glycans and derivatives, and converts them to various notations
   Direct weblink | Citation link.

Symbol Nomenclature ☝

Downloadable files: Drawing format | Presentation/Slide format

Each symbol represents a specific monosaccharide or class of monosaccharides found in nature. Hover over the symbol with pointer to see the full monosaccharide name. Click on a symbol to link to the corresponding PubChem entry. Symbols can also be copied with embedded links from the table using right/control-click or highlight-copy (highlight a symbol, then control-c [on pc], or command⌘-c [on mac]). However links may not copy in some browsers. Symbols with embedded PubChem URLs are therefore also available in the presentation/slide format attachments (see links above the table). A high-quality SVG object file is also provided.

Table 1. Monosaccharide symbol nomenclature (Download TSV data file) ☝

SHAPE	White (Generic)	Blue	Green	Yellow	Orange	Pink	Purple	Light Blue	Brown	Red
Filled Circle	Hexose	Glc	Man	Gal	Gul	Alt	All	Tal	Ido
Filled Square	HexNAc	GlcNAc	ManNAc	GalNAc	GulNAc	AltNAc	AllNAc	TalNAc	IdoNAc
Crossed Square	Hexosamine	GlcN	ManN	GalN	GulN	AltN	AllN	TalN	IdoN
Divided Diamond	Hexuronate	GlcA	ManA	GalA	GulA	AltA	AllA	TalA	IdoA
Filled Triangle	Deoxyhexose	Qui	Rha		6dGul	6dAlt		6dTal		Fuc
Divided Triangle	DeoxyhexNAc	QuiNAc	RhaNAc			6dAltNAc		6dTalNAc		FucNAc
Flat Rectangle	Di-deoxyhexose	Oli	Tyv		Abe	Par	Dig	Col
Filled Star	Pentose		Ara	Lyx	Xyl	Rib
Filled Diamond	3-deoxy-nonulosonic acids		Kdn				Neu5Ac	Neu5Gc	Neu	Sia
Flat Diamond	3,9-dideoxy-nonulosonic acids		Pse	Leg		Aci		4eLeg
Flat Hexagon	Unknown	Bac	LDmanHep	Kdo	Dha	DDmanHep	MurNAc	MurNGc	Mur
Pentagon	Assigned	Api	Fru	Tag	Sor	Psi

Notes

1. General: The monosaccharide symbols presented here are from the Fourth Edition of the Essentials of Glycobiology. They are extended from the symbols in the Second Edition to cover a wider range of monosaccharides found in nature. While previous versions allowed conversion of monosaccharide symbols to black and white representation, this is no longer possible. A listing of abbreviated, full, and complete names of all assigned monosaccharides is provided in Table 4. Selected examples depicting SNFG usage are presented below, for various living organisms.
2. Drawing recommendations: All downloadable symbols follow CMYK colors as shown in Table 2, which were generated in Adobe Illustrator. Recommended CMYK to RGB conversion is also provided. While there is no hard rule, glycans are typically sketched to orient their non-reducing end in either the left or upward direction.
3. Shape, color and symbol orientation: Shapes and colors are completely consistent with stereochemistry only for hexoses, hexosamines, N-acetylhexosamines, hexuronic acids, and pentoses. Shapes only are consistent for deoxyhexoses, deoxy-N-acetylhexosamines, dideoxyhexoses, and nonulosonic acids. Avoid rotating the symbols.
4. Ring configuration: A colored symbol encodes a defined monosaccharide (including D or L) independent of rotation or mirroring. Pyranose form is assumed by default for all monosaccharides except Api. Symbols used at the reducing end without specification of α/β represent all forms that a monosaccharide can adopt due to mutarotation. A few monosaccharides have absolute configurations implicitly specified in their name (D for Abe, Bac, Dha, Kdo, Mur, Par, Tyv; L for Col; DD for Kdn, Neu, Leg, 4eLeg; LL for Pse, Aci; LD for 8eLeg; DL for 8eAci). For all other residues, absolute configuration is assumed by default: L for Ara, Fuc, Ido, IdoA, Rha, Alt, AltA, Sor, Api; and D for other monosaccharides.
   Less common configurations need to be stated in a figure legend or by adding letters inside the symbol (e.g., adding D or L to the symbol). Epimers at C8 of nonulosonic acids can be indicated by adding "8D" or "8L" inside the symbol (8L for 8eLeg, 8D for 8eAci). Furanose rings can be indicated by adding an italicized "f", alditols indicated with an italicized "o", and open ring at the reducing end using "a" inside the symbol. Other modifications of the monosaccharide base stereochemistry can be specified using two letters within the monosaccharide symbol: "en" for didehydro, "an" for anhydro, "on" for lactone and "am" for lactam. The default carbon positions for these modifications in sialic acids are at 2-3 for en, 2-7 for an, 1-7 for on, and 1-5 for am. Departures from this default should be specified in figure footnotes/legends.
5. Linkage presentation: Anomeric notation and destination linkage can be indicated in IUPAC style in figures, with or without a dash and with or without the originating carbon number (but with no commas or spacing) (e.g., Neu5Acα2-3Galβ1-4GlcNAc, Neu5Acα3Galβ4GlcNAc, or equivalents in symbol drawings).
   All monosaccharide glycosidic linkages are assumed to originate from C-1, except for 2-ketoses, which are assumed to be linked from C-2. Linkages in the schematics should be sorted to appear in the clockwise order, with the linkages to the lowest carbon number occurring to the left. Optionally, these may also follow the Oxford System that embeds both the specificity and anomericity of the monosaccharide linkages. Dual linkages (e.g., an outgoing linkage from an aldose in open form) can be shown by double lines. Linkages involving carbon-carbon bond (e.g., in C-glycosides) can be shown in different color. An internal phosphodiester can be shown with -P- between the symbols for the linked monosaccharides, with linkage positions specified.
6. Nonulosonic acids (including sialic acids): Specific symbols are provided for the core sialic acids (3-deoxy-non-2-ulosonic acids / 3-deoxy-nonulosonic acids): Neu, Neu5Ac, Neu5Gc, and Kdn. Symbols are also available for the core sialic-acid like 3,9-dideoxy-non-2-ulosonic acids / 3,9-dideoxy-nonulosonic acids: pseudaminic acid (Pse), legionaminic acid (Leg), acinetaminic acid (Aci) and 4-epi-legionaminic acid (4eLeg). Modifications to these monosaccharides may be indicated in diagrams (e.g., 9Ac for 9-O-acetylation). A red diamond can be used for any Sia (sialic acid, type unknown, whether Neu5Gc or Neu5Ac, or any of the other >90 forms known to date). The NulO concept page provides a detailed catalog of currently known NulOs, primary citations and related database links.
7. Carbohydrate modifications: Modification of any base monosaccharide by chemical substituent is described using a number indicating the linkage position and text indicating the substituent-type, e.g., 3S for 3-O-sulfate, 6P for 6-O-phosphate, and 4,6Pyr for 4,6-pyruvyl [4,6-O-(1-carboxyethylidene)]. The abbreviated text used to describe common substituents is listed in Table 3, along with associated chemical drawings. The following guidelines are used to describe monosaccharide substituents:
   i) Substituent names and abbreviations are guided by IUPAC convention, but common names are also allowed to keep with usage in the field and to enhance human readability.
   ii) Substituent abbreviations are ideally 2-3 letters long. To save space, subscripts maybe dropped, e.g. Kdn4,7Ac₂ is pictorially depicted as a green diamond with 4,7Ac rather than 4,7Ac₂.
   iii) Avoid numbers when describing substituents if possible, in order to reduce confusion with number used to depict linkage position. If numbers are necessary, then the substituent should be enclosed within parenthesis.
   iv) Substituents should appear in alphabetical order based on Table 3. If the same modification appears at multiple carbon-locations this should be presented in numerical order. If the position of modification is unknown, this may be indicated using ?, e.g. ?Me if the methyl location of substituent is not known.
   v) The attachment of a substituent to the hydroxyl group on the base monosaccharide would result in an O-linked substituent and similar modification on amine would indicate N-linked addition. Thus, Neu4,5Ac₂8Me indicates O-acetylation at C4 of Neu (neuraminic acid), N-acetyl at C5, and O-methyl at C8.
   vi). Substituents may be concatenated to indicate multiple modifications, with position indicated for the first substituent, e.g. 'Neu5(Gc2Ac)' depicting the C5 modification of Neu by a glycolyl group which is further modified by O-acetyl at C2 of the glycolyl substituent. If a given string concatenation results in a non-unique chemical description, the exact chemical structure should be provided using IUPAC rules.
   vii) The presence of variable amounts of substituents can be indicated using +/- symbol or by indicating % presence if known, e.g. "60% 3Ac" to indicate presence of 3Ac on 60% of a residue or repeating unit.
   viii) Substituents not in Table 3 may be included using above guidelines with footnotes describing the entity type/chemistry. A symbol (like *, † or ‡) above the SNFG monosaccharide and associated footnote may also be used when text describing substituent becomes large.
8. Amino substitution: The position for N-substitution is assumed in the base symbol to be at the most common site(s), for example the 2-position of glucosamine, the 5-position of neuraminic acid, and the 5 & 7 positions of pseudaminic acid. By default, it is assumed that these N-substituted groups are modified, e.g., NS for N-sulfate group on glucosamine is assumed to be at the 2-position. For monosaccharides in which nitrogen is not implicit in its structure, add a number to the N (e.g., Rha4N is shown as a green triangle with 4N attached). Additionally, atypical acetamido groups may be represented using NAc (e.g. Fuc4NAc is shown using red triangle with 4NAc attached).
9. Ambiguous linkage position and glycan mixtures: Brackets (either straight or curly) indicate attachment of specific monosaccharides or structures to any residue within the glycan. Restrictions on the nature of attachment are specified by including linkage data on the bond outside the brackets. Constraints on attachment site are shown using asterisk followed by a number (*#), specified both on the bond and its attachment site(s). Such renderings are used to indicate ambiguity in the structure of a specific glycan. By extension, glycan mixtures may be depicted by including [number range] along the bond as shown in the examples.
10. Ambiguous monosaccharides: White symbols based on the standard shapes designate monosaccharides with unknown/undefined stereochemistry (e.g., a white circle designates a hexose, type not defined, or a white diamond, any deoxynonulosonic acid). Other unknown or partially defined monosaccharides may be represented using a white flat hexagon.
11. Structures not present in table and non-glycan assignments: Monosaccharides absent in Table 1 or modifications that cannot be represented using the above rules, may be indicated using a single non-italicized letter (A..Z) within an SNFG white symbol, with additional details provided in figure footnote or legends. The choice of white symbol to use should fit the generic type if possible: circle for hexose, triangle for deoxyhexose etc.; otherwise, the white pentagon should be used. Any black shape can be used to depict non-monosaccharide structures and detailed definitions should be provided in figure legends. More complicated modifications of the SNFG are discouraged, and if these modifications are made should not be referred to as following the SNFG nomenclature.

Examples of Glycan Symbol Nomenclature ☝

Table 2. CMYK and RGB color assignments (Download TSV data file) ☝

Color	CMYK settings	RGB settings
White	0/0/0/0	255/255/255
Blue	100/50/0/0	0/114/188
Green	100/0/100/0	0/166/81
Yellow	0/15/100/0	255/212/0
Light blue	41/5/3/0	143/204/233
Pink	0/47/24/0	246/158/161
Purple	38/88/0/0	165/67/153
Brown	32/48/76/13	161/122/77
Orange	0/65/100/0	244/121/32
Red	0/100/100/0	237/28/36

* CMYK colors are presented as %

Table 3. Monosaccharide substituents and abbreviations* (Download TSV data file) ☝

Abbreviation	Substituent
Ac	acetyl
Ala	D-alanyl
Ala2Ac	N-acetyl-D-alanyl
Am	N-acetimidoyl
AmMe	N-(N-methyl-acetimidoyl)
AmMe2	N-(N,N-dimethyl-acetimidoyl)
Fo	formyl
Gc	glycolyl
Gln2Ac	N-acetyl-glutaminyl
5Glu2Me	N-methyl-5-glutamyl
Gly	glycyl
Gr	glyceryl
Gr2,3Me2	2,3-di-O-methyl-glyceryl
4Hb	4-hydroxybutyryl
3,4Hb	3,4-dihydroxybutyryl
3RHb	(R)-3-hydroxybutyryl
3SHb	(S)-3-hydroxybutyryl
Lt	lactyl
Me	methyl
N	amino
NAc	N-acetyl
P	phosphate
Py	pyruvyl
Pyr	1-carboxyethylidene
S	sulfate
Tau	tauryl

*If multiple substituents are attached to a single monosaccharide, in the SNFG rendering, the substituent abbreviations appear in alphabetical order.

Chemical structure of substituents ☝

Table 4. Monosaccharide abbreviations and names (Download TSV data file) ☝

Abbreviation	Short Name	Systematic name	Structure	CID	SID
4eLeg	4-epi-Legionaminic acid	5,7-Diamino-3,5,7,9-tetradeoxy-D-glycero-D-talo-non-2-ulopyranosonic acid		126961780	252089092
6dAlt	6-Deoxy-L-altrose	6-Deoxy-L-altropyranose		12302958	252300980
6dAltNAc	N-Acetyl-6-deoxy-L-altrosamine	2-Acetamido-2,6-dideoxy-L-altropyranose		126961777	336286661
6dGul	6-Deoxy-D-gulose	6-Deoxy-D-gulopyranose		12302960	336286660
6dTal	6-Deoxy-D-talose	6-Deoxy-D-talopyranose		44119431	252301016
6dTalNAc	N-Acetyl-6-deoxy-D-talosamine	2-Acetamido-2,6-dideoxy-D-talopyranose		126961778	336286662
8eAci	8-epi-Acinetaminic acid	5,7-Diamino-3,5,7,9-tetradeoxy-D-glycero-L-altro-non-2-ulopyranosonic acid		168009119	480493268
8eLeg	8-epi-Legionaminic acid	5,7-Diamino-3,5,7,9-tetradeoxy-L-glycero-D-galacto-non-2-ulopyranosonic acid		168009112	252090150
Abe	Abequose	3,6-Dideoxy-D-xylo-hexopyranose		160540	252091216
Aci	Acinetaminic acid	5,7-Diamino-3,5,7,9-tetradeoxy-L-glycero-L-altro-non-2-ulopyranosonic acid		126961779	252089094
All	D-Allose	D-Allopyranose		439507	251973843
AllA	D-Alluronic acid	D-Allopyranuronic acid		6602103	251973908
AllN	D-Allosamine	2-Amino-2-deoxy-D-allopyranose		6915732	251973859
AllNAc	N-Acetyl-D-allosamine	2-Acetamido-2-deoxy-D-allopyranose		10944029	251973851
Alt	L-Altrose	L-Altropyranose		10219674	251973845
AltA	L-Altruronic acid	L-Altropyranuronic acid		56845780	252300979
AltN	L-Altrosamine	2-Amino-2-deoxy-L-altropyranose		6602094	251973836
AltNAc	N-Acetyl-L-altrosamine	2-Acetamido-2-deoxy-L-altropyranose		44717159	251973853
Api	L-Apiose	3-C-(Hydroxymethyl)-L-erythro-tetrofuranose		12306753	252106892
Ara	L-Arabinose	L-Arabinopyranose		439195	252089084
Bac	Bacillosamine	2,4-Diamino-2,4,6-trideoxy-D-glucopyranose		54029194	252091138
Col	Colitose	3,6-Dideoxy-L-xylo-hexopyranose		12303780	252091214
DDmanHep	D-glycero-D-manno-Heptose	D-glycero-D-manno-Heptopyranose		53681436	252301021
Dha	3-Deoxy-D-lyxo-heptulosaric acid	3-Deoxy-D-lyxo-hept-2-ulopyranosaric acid		15608515	252090263
Dig	D-Digitoxose	2,6-Dideoxy-D-ribo-hexopyranose		2723626	252301018
Fru	D-Fructose	D-arabino-Hex-2-ulopyranose		2723872	252106896
Fuc	L-Fucose	6-Deoxy-L-galactopyranose		17106	251973912
FucNAc	N-Acetyl-L-fucosamine	2-Acetamido-2,6-dideoxy-L-galactopyranose		91810489	252089082
Gal	D-Galactose	D-Galactopyranose		6036	251973840
GalA	D-Galacturonic acid	D-Galactopyranuronic acid		439215	251973905
GalN	D-Galactosamine	2-Amino-2-deoxy-D-galactopyranose		24154	251973856
GalNAc	N-Acetyl-D-galactosamine	2-Acetamido-2-deoxy-D-galactopyranose		35717	251973848
Glc	D-Glucose	D-Glucopyranose		5793	251973837
GlcA	D-Glucuronic acid	D-Glucopyranuronic acid		94715	251973835
GlcN	D-Glucosamine	2-Amino-2-deoxy-D-glucopyranose		439213	251973854
GlcNAc	N-Acetyl-D-glucosamine	2-Acetamido-2-deoxy-D-glucopyranose		439174	251973846
Gul	D-Gulose	D-Gulopyranose		441033	251973842
GulA	D-Guluronic acid	D-Gulopyranuronic acid		11788788	251973907
GulN	D-Gulosamine	2-Amino-2-deoxy-D-gulopyranose		9920528	251973858
GulNAc	N-Acetyl-D-gulosamine	2-Acetamido-2-deoxy-D-gulopyranose		13201633	251973850
Ido	L-Idose	L-Idopyranose		11030410	251973844
IdoA	L-Iduronic acid	L-Idopyranuronic acid		441039	251973909
IdoN	L-Idosamine	2-Amino-2-deoxy-L-idopyranose		91864695	251973839
IdoNAc	N-Acetyl-L-idosamine	2-Acetamido-2-deoxy-L-idopyranose		13201636	251973852
Kdn	2-Keto-3-deoxy-nononic acid	3-Deoxy-D-glycero-D-galacto-non-2-ulopyranosonic acid		13991616	252089089
Kdo	3-Deoxy-D-manno-octulosonic acid	3-Deoxy-D-manno-oct-2-ulopyranosonic acid		10857507	252090262
Leg	Legionaminic acid	5,7-Diamino-3,5,7,9-tetradeoxy-D-glycero-D-galacto-non-2-ulopyranosonic acid		70678967	252089090
LDmanHep	L-glycero-D-manno-Heptose	L-glycero-D-manno-Heptopyranose		21120522	252301020
Lyx	D-Lyxose	D-Lyxopyranose		439240	252089085
Man	D-Mannose	D-Mannopyranose		18950	251973838
ManA	D-Mannuronic acid	D-Mannopyranuronic acid		439630	251973904
ManN	D-Mannosamine	2-Amino-2-deoxy-D-mannopyranose		440049	251973855
ManNAc	N-Acetyl-D-mannosamine	2-Acetamido-2-deoxy-D-mannopyranose		439281	251973847
Mur	Muramic acid	2-Amino-3-O-[(R)-1-carboxyethyl]-2-deoxy-D-glucopyranose		441038	252301022
MurNAc	N-Acetylmuramic acid	2-Acetamido-3-O-[(R)-1-carboxyethyl]-2-deoxy-D-glucopyranose		5462244	252091139
MurNGc	N-Glycolylmuramic acid	3-O-[(R)-1-Carboxyethyl]-2-deoxy-2-hydroxyacetamido-D-glucopyranose		91810748	252090151
Neu	Neuraminic acid	5-Amino-3,5-dideoxy-D-glycero-D-galacto-non-2-ulopyranosonic acid		441037	252301019
Neu5Ac	N-Acetylneuraminic acid	5-Acetamido-3,5-dideoxy-D-glycero-D-galacto-non-2-ulopyranosonic acid		439197	252089093
Neu5Gc	N-Glycolylneuraminic acid	3,5-Dideoxy-5-hydroxyacetamido-D-glycero-D-galacto-non-2-ulopyranosonic acid		440001	252089091
Oli	Olivose	2,6-Dideoxy-D-arabino-hexopyranose		10888063	252301017
Par	Paratose	3,6-Dideoxy-D-ribo-hexopyranose		12303783	252106894
Pse	Pseudaminic acid	5,7-Diamino-3,5,7,9-tetradeoxy-L-glycero-L-manno-non-2-ulopyranosonic acid		101137651	252089088
Psi	D-Psicose	D-ribo-Hex-2-ulopyranose		441036	252106897
Qui	D-Quinovose	6-Deoxy-D-glucopyranose		439746	251973910
QuiNAc	N-Acetyl-D-quinovosamine	2-Acetamido-2,6-dideoxy-D-glucopyranose		11954187	251973913
Rha	L-Rhamnose	6-Deoxy-L-mannopyranose		25310	251973911
RhaNAc	N-Acetyl-L-rhamnosamine	2-Acetamido-2,6-dideoxy-L-mannopyranose		91807222	251973914
Rib	D-Ribose	D-Ribopyranose		10975657	252089083
Sia	Sialic acid	Sialic acid residue of unspecified type			341861327
Sor	L-Sorbose	L-xylo-Hex-2-ulopyranose		439192	252091215
Tag	D-Tagatose	D-lyxo-Hex-2-ulopyranose		439312	252106895
Tal	D-Talose	D-Talopyranose		441035	251973841
TalA	D-Taluronic acid	D-Talopyranuronic acid		11298488	251973906
TalN	D-Talosamine	2-Amino-2-deoxy-D-talopyranose		9834117	251973857
TalNAc	N-Acetyl-D-talosamine	2-Acetamido-2-deoxy-D-talopyranose		57376616	251973849
Tyv	Tyvelose	3,6-Dideoxy-D-arabino-hexopyranose		12303782	252106893
Xyl	D-Xylose	D-Xylopyranose		135191	252089086

Clicking on the abbreviation leads to the corresponding entry in PubChem

Updates ☝

Feburary 26, 2024 (Version 2.0.4)

1. Add monosaccharide depictions and corresponding identifiers, CIDs and SIDs.
2. Add table data download in TSV format.

August 20, 2023 (Version 2.0.3)

1. Minor edits made to the chemical structures in the substituent table.
2. SNFG reference collection initiated at NCBI-pubchem.

October 19, 2022 (Version 2.0.2)

1. SNFG adopts the creative commons CC0 license. This formalizes the open-source nature of this community-driven endeavor.

September 1, 2022 (Version 2.0.1)

1. Minor edits to clarify footnotes #7 and #8, and update to one of the SNFG examples.

June 27, 2022 (Version 2.0)

1. SNFG expanded to describe sialic acid and sialic acid-like monosaccharides.
2. Substituent table added, along with figure describing their chemical structures.
3. SNFG notes expanded to include new guidelines on how to describe substituents.
4. SNFG examples and presentation slides redone with more examples, and refinements.
5. SNFG Table 1 redone with higher resolution images.
6. SNFG versioning initiated in order to aid compliance with FAIR principles.
7. Rules added to describe open ring configurations (aldehyde, ketone) at free reducing end.

February 4, 2020 (Version 1.5)

1. Rules added for specification of symbol and bond orientation.

November 20, 2019 (Version 1.4)

1. SNFG now provides guidelines to depict ambiguous linkages and glycan mixtures using bracket notation.

May 9, 2019 (Version 1.3)

1. Footnote 7 modified to accommodate variable modifications.
2. More SNFG usage examples added.

January 22, 2019 (Version 1.2)

1. SNFG page reorganized with new examples from mammals, yeast, slime mold, insects, bacteria and plants.
2. The new examples focus on how to present carbohydrate structures in diverse organisms and ambiguous monosaccharide assignments.
3. Number of footnotes reduced from 28 to 10, and thematically organized in order to simplify usage.
4. Single non-italicized letter is now allowed in white symbols to help describe monosaccharides that are not part of the SNFG table and that cannot be described using existing footnotes.
5. SNFG Discussion Group list updated.

June 5, 2017 (Version 1.1)

1. SNFG Discussion Group Listing added.
2. White diamond now indicates any deoxynonulosonic acid.
3. Flattened diamond introduced for any dideoxynonulosonic acid.
4. Additional symbols added for 6dGul, 6dAltNAc, 6dTalNAc, Pse, Leg, Aci and 4eLeg.
5. Drawglycan-SNFG and Glycanbuilder 2-SNFG adopted, link to web site provided.
6. Updates to Appendix 52A. Organizations and publications adopting SNFG.
7. RGB color code provided in addition to CMYK
8. Multiple minor corrections and additions to nomenclature and rules of display.

August 31, 2016 (Version 1.0)

1. Link to new Appendix 52A. Organizations and Publications Adopting SNFG.
2. Red diamond introduced for Sia (sialic acid, type unspecified). White diamond indicates any nonulosonic acid.
3. A 3D Symbol Nomenclature for Glycans (3D-SNFG) adopted, link to web site provided.
4. Multiple minor corrections and additions to nomenclature and rules of display.

License ☝

The SNFG is distributed using the public domain CC0 license (https://creativecommons.org/publicdomain/zero/1.0/). This means that users are free to copy, distribute, display and make commercial use of the standard and data shown on this page.