Canonical Allele Identifier: CA1080271829

Gene:

Linked Data

• dbSNP Id: rs1780062399
• gnomAD v3: 5-113660930-A-G
• gnomAD v4: 5-113660930-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113660930A>G , CM000667.2:g.113660930A>G	GRCh38
NC_000005.9:g.112996627A>G , CM000667.1:g.112996627A>G	GRCh37
NC_000005.8:g.113024526A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001742841.1:n.59+27566A>G