Canonical Allele Identifier: CA11075013
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016274C>T , CM000664.2:g.88016274C>T GRCh38
NC_000002.11:g.88315793C>T , CM000664.1:g.88315793C>T GRCh37
NC_000002.10:g.88096908C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.619C>T
XR_940336.3:n.619C>T