ClinVar

NM_002109.6(HARS1):c.951+19G>A

Gene:

HARS1:histidyl-tRNA synthetase 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

5q31.3

Genomic location:

• Chr5: 140676970 (on Assembly GRCh38)
• Chr5: 140056555 (on Assembly GRCh37)

Preferred name:

NM_002109.6(HARS1):c.951+19G>A

HGVS:

• NC_000005.10:g.140676970C>T
• NG_032158.1:g.19417G>A
• NM_001258040.3:c.831+19G>A
• NM_001258041.3:c.891+19G>A
• NM_001258042.3:c.771+19G>A
• NM_001289092.2:c.729+19G>A
• NM_001289093.2:c.609+19G>A
• NM_001289094.2:c.864+19G>A
• NM_002109.6:c.951+19G>AMANE SELECT
• LRG_1374t1:c.951+19G>A
• LRG_1374:g.19417G>A
• NC_000005.9:g.140056555C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs73271581

NCBI 1000 Genomes Browser:

rs73271581

Molecular consequence:

• NM_001258040.3:c.831+19G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001258041.3:c.891+19G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001258042.3:c.771+19G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001289092.2:c.729+19G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001289093.2:c.609+19G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001289094.2:c.864+19G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_002109.6:c.951+19G>A - intron variant - [Sequence Ontology: SO:0001627]