Canonical Allele Identifier: CA11622985
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39262973G>A , CM000665.2:g.39262973G>A GRCh38
NC_000003.11:g.39304464G>A , CM000665.1:g.39304464G>A GRCh37
NC_000003.10:g.39279468G>A NCBI36
NG_016362.1:g.23763C>T

Transcript Alleles

HGVS Amino-acid Change
XR_001740660.2:n.2490G>A