Canonical Allele Identifier: CA15517698
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388483G>A , CM000669.2:g.97388483G>A GRCh38
NC_000007.13:g.97017795G>A , CM000669.1:g.97017795G>A GRCh37
NC_000007.12:g.96855731G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59836C>T