Canonical Allele Identifier: CA1817441872
Gene:

Linked Data

dbSNP Id: rs1812776583

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125478546C>A , CM000670.2:g.125478546C>A GRCh38
NC_000008.10:g.126490788C>A , CM000670.1:g.126490788C>A GRCh37
NC_000008.9:g.126559970C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+5232C>A