Canonical Allele Identifier: CA896967427

Gene:

Linked Data

• dbSNP Id: rs1381217061
• gnomAD v3: 3-109743622-A-G
• gnomAD v4: 3-109743622-A-G
• MyVariant Identifiers: chr3:g.109462469A>G (hg19) ; chr3:g.109743622A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.109743622A>G , CM000665.2:g.109743622A>G	GRCh38
NC_000003.11:g.109462469A>G , CM000665.1:g.109462469A>G	GRCh37
NC_000003.10:g.110945159A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924325.1:n.142+63427A>G