Canonical Allele Identifier: CA50218043

Gene:

Linked Data

• dbSNP Id: rs956205982
• gnomAD v3: 2-67637565-T-A
• gnomAD v4: 2-67637565-T-A
• MyVariant Identifiers: chr2:g.67864697T>A (hg19) ; chr2:g.67637565T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.67637565T>A , CM000664.2:g.67637565T>A	GRCh38
NC_000002.11:g.67864697T>A , CM000664.1:g.67864697T>A	GRCh37
NC_000002.10:g.67718201T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001739524.1:n.65+13401A>T