Canonical Allele Identifier: CA15098853
Gene:

Linked Data

dbSNP Id: rs7511868

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161493541G>A , CM000663.2:g.161493541G>A GRCh38
NC_000001.10:g.161463331G>A , CM000663.1:g.161463331G>A GRCh37
NC_000001.9:g.159729955G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922214.1:n.1933G>A
XR_922214.2:n.2882G>A