Canonical Allele Identifier: CA1106753699

Gene:

Linked Data

• dbSNP Id: rs1795646715
• gnomAD v3: 7-124306388-T-A
• gnomAD v4: 7-124306388-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.124306388T>A , CM000669.2:g.124306388T>A	GRCh38
NC_000007.13:g.123946442T>A , CM000669.1:g.123946442T>A	GRCh37
NC_000007.12:g.123733678T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_002956584.1:n.73-90T>A