Canonical Allele Identifier: CA153770468
Gene:

Linked Data

dbSNP Id: rs533361493

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.9816743T>A , CM000669.2:g.9816743T>A GRCh38
NC_000007.13:g.9856372T>A , CM000669.1:g.9856372T>A GRCh37
NC_000007.12:g.9822897T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927024.1:n.209+50047A>T
XR_927025.1:n.323+50047A>T
XR_927026.1:n.209+50047A>T
XR_927026.2:n.209+50047A>T