Canonical Allele Identifier: CA137102506
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33522105G>A , CM000668.2:g.33522105G>A GRCh38
NC_000006.11:g.33489882G>A , CM000668.1:g.33489882G>A GRCh37
NC_000006.10:g.33597860G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743876.1:n.18-2614C>T