Canonical Allele Identifier: CA1080271816

Gene:

Linked Data

• dbSNP Id: rs1716915398
• gnomAD v3: 5-113660889-G-A
• gnomAD v4: 5-113660889-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113660889G>A , CM000667.2:g.113660889G>A	GRCh38
NC_000005.9:g.112996586G>A , CM000667.1:g.112996586G>A	GRCh37
NC_000005.8:g.113024485G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001742841.1:n.59+27525G>A