Canonical Allele Identifier: CA770000082

Gene:

Linked Data

• dbSNP Id: rs1462935330
• gnomAD v3: 2-52722461-T-C
• gnomAD v4: 2-52722461-T-C
• MyVariant Identifiers: chr2:g.52949599T>C (hg19) ; chr2:g.52722461T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.52722461T>C , CM000664.2:g.52722461T>C	GRCh38
NC_000002.11:g.52949599T>C , CM000664.1:g.52949599T>C	GRCh37
NC_000002.10:g.52803103T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_002959384.1:n.796A>G