Canonical Allele Identifier: CA2777062302
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388377C>G , CM000669.2:g.97388377C>G GRCh38
NC_000007.13:g.97017689C>G , CM000669.1:g.97017689C>G GRCh37
NC_000007.12:g.96855625C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59730G>C