Canonical Allele Identifier: CA81296275

Gene:

Linked Data

• dbSNP Id: rs890890580
• gnomAD v3: 3-109743535-A-T
• gnomAD v4: 3-109743535-A-T
• MyVariant Identifiers: chr3:g.109462382A>T (hg19) ; chr3:g.109743535A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.109743535A>T , CM000665.2:g.109743535A>T	GRCh38
NC_000003.11:g.109462382A>T , CM000665.1:g.109462382A>T	GRCh37
NC_000003.10:g.110945072A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924325.1:n.142+63340A>T