Canonical Allele Identifier: CA2561136986
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756697G>A , CM000680.2:g.31756697G>A GRCh38
NC_000018.9:g.29336660G>A , CM000680.1:g.29336660G>A GRCh37
NC_000018.8:g.27590658G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5442G>A