Canonical Allele Identifier: CA13214168
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697617T>A , CM000672.2:g.8697617T>A GRCh38
NC_000010.10:g.8739580T>A , CM000672.1:g.8739580T>A GRCh37
NC_000010.9:g.8779586T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930641.1:n.33-27816A>T