Canonical Allele Identifier: CA1985859956
Gene:

Linked Data

dbSNP Id: rs1857709631

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.80851718A>G , CM000673.2:g.80851718A>G GRCh38
NC_000011.9:g.80562761A>G , CM000673.1:g.80562761A>G GRCh37
NC_000011.8:g.80240409A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247272.2:n.124+60573T>C