Canonical Allele Identifier: CA2774472378
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13400672G>A , CM000669.2:g.13400672G>A GRCh38
NC_000007.13:g.13440297G>A , CM000669.1:g.13440297G>A GRCh37
NC_000007.12:g.13406822G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745097.1:n.147+90349G>A