Canonical Allele Identifier: CA93117901
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578134G>A , CM000666.2:g.12578134G>A GRCh38
NC_000004.11:g.12579758G>A , CM000666.1:g.12579758G>A GRCh37
NC_000004.10:g.12188856G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925406.1:n.106+31208C>T
XR_001741374.1:n.254+44521C>T
XR_925406.3:n.140+31208C>T