Canonical Allele Identifier: CA896967442

Gene:

Linked Data

• dbSNP Id: rs1364755280
• gnomAD v3: 3-109743646-A-G
• gnomAD v4: 3-109743646-A-G
• MyVariant Identifiers: chr3:g.109462493A>G (hg19) ; chr3:g.109743646A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.109743646A>G , CM000665.2:g.109743646A>G	GRCh38
NC_000003.11:g.109462493A>G , CM000665.1:g.109462493A>G	GRCh37
NC_000003.10:g.110945183A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_924325.1:n.142+63451A>G