Canonical Allele Identifier: CA1233161535
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.638144G>A , CM000664.2:g.638144G>A GRCh38
NC_000002.11:g.638144G>A , CM000664.1:g.638144G>A GRCh37
NC_000002.10:g.628144G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510438.1:c.*572+760G>A XP_011508740.1:n.*572+760G>A