Canonical Allele Identifier: CA1092790784

Gene:

Linked Data

• dbSNP Id: rs1771941491
• gnomAD v3: 6-105805172-A-G
• gnomAD v4: 6-105805172-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.105805172A>G , CM000668.2:g.105805172A>G	GRCh38
NC_000006.11:g.106253047A>G , CM000668.1:g.106253047A>G	GRCh37
NC_000006.10:g.106359740A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_942835.1:n.510+24885T>C
XR_001744274.1:n.438+24885T>C
XR_001744275.1:n.337+24885T>C