Canonical Allele Identifier: CA81296279
Gene:

Linked Data

dbSNP Id: rs780547461

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743558G>A , CM000665.2:g.109743558G>A GRCh38
NC_000003.11:g.109462405G>A , CM000665.1:g.109462405G>A GRCh37
NC_000003.10:g.110945095G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924325.1:n.142+63363G>A