Canonical Allele Identifier: CA896967440

Gene:

Linked Data

• dbSNP Id: rs1422469582
• gnomAD v3: 3-109743645-T-C
• gnomAD v4: 3-109743645-T-C
• MyVariant Identifiers: chr3:g.109462492T>C (hg19) ; chr3:g.109743645T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.109743645T>C , CM000665.2:g.109743645T>C	GRCh38
NC_000003.11:g.109462492T>C , CM000665.1:g.109462492T>C	GRCh37
NC_000003.10:g.110945182T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_924325.1:n.142+63450T>C