Canonical Allele Identifier: CA1985859960
Gene:

Linked Data

dbSNP Id: rs1857709677

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.80851723C>A , CM000673.2:g.80851723C>A GRCh38
NC_000011.9:g.80562766C>A , CM000673.1:g.80562766C>A GRCh37
NC_000011.8:g.80240414C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247272.2:n.124+60568G>T