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Chromosome 2 - NC_000002.12
Genomic Sequence: NC_000002.12 Chromosome 2 Reference GRCh38.p14 Primary Assembly NW_025791760.1 Chromosome 2 Reference GRCh38.p14 PATCHES NC_060926.1 Chromosome 2 Alternate T2T-CHM13v2.0 NC_000002.11 Chromosome 2 Reference GRCh37.p13 Primary Assembly
Go to nucleotide: Graphics FASTA GenBank
See all (81) citations in PubMed
Find tests for this gene in the NIH Genetic Testing Registry (GTR)
Review eQTL and phenotype association data in this region using PheGenI
See variants in ClinVar
See studies and variants in dbVar
See Variation Viewer (GRCh37.p13)
See Variation Viewer (GRCh38)
Go to the HIV-1, Human Interaction Database
NEW Try the new Transcript table
These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.
NM_001034914.2 → NP_001030086.1 calsenilin isoform 2
See identical proteins and their annotated locations for NP_001030086.1
Status: REVIEWED
NM_013434.5 → NP_038462.1 calsenilin isoform 1
See identical proteins and their annotated locations for NP_038462.1
The following sections contain reference sequences that belong to a specific genome build. Explain
This section includes genomic Reference Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate assemblies. Model RNAs and proteins are also reported here.
NC_000002.12 Reference GRCh38.p14 Primary Assembly
NW_025791760.1 Reference GRCh38.p14 PATCHES
NC_060926.1 Alternate T2T-CHM13v2.0
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