Canonical Allele Identifier: CA761272665

Gene:

Linked Data

• dbSNP Id: rs1480741340
• gnomAD v3: 2-17844069-T-A
• gnomAD v4: 2-17844069-T-A
• MyVariant Identifiers: chr2:g.18025336T>A (hg19) ; chr2:g.17844069T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.17844069T>A , CM000664.2:g.17844069T>A	GRCh38
NC_000002.11:g.18025336T>A , CM000664.1:g.18025336T>A	GRCh37
NC_000002.10:g.17888817T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_939764.2:n.447+3625A>T