Canonical Allele Identifier: CA1740470123

Gene:

Linked Data

• dbSNP Id: rs899649429
• gnomAD v4: 7-124306361-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.124306361A>G , CM000669.2:g.124306361A>G	GRCh38
NC_000007.13:g.123946415A>G , CM000669.1:g.123946415A>G	GRCh37
NC_000007.12:g.123733651A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_002956584.1:n.73-117A>G