Canonical Allele Identifier: CA36468615
Gene:

Linked Data

dbSNP Id: rs947211

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.205783537A>G , CM000663.2:g.205783537A>G GRCh38
NC_000001.10:g.205752665A>G , CM000663.1:g.205752665A>G GRCh37
NC_000001.9:g.204019288A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922472.1:n.889A>G