Canonical Allele Identifier: CA287548625
Gene:

Linked Data

dbSNP Id: rs927618480

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137653T>A , CM000679.2:g.8137653T>A GRCh38
NC_000017.10:g.8040971T>A , CM000679.1:g.8040971T>A GRCh37
NC_000017.9:g.7981696T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934202.1:n.183-1196T>A
XR_934203.1:n.70-1824T>A
XR_934202.2:n.414-1196T>A