Canonical Allele Identifier: CA2636471289
Gene: TOP3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18271396G>A , CM000679.2:g.18271396G>A GRCh38
NC_000017.10:g.18174710G>A , CM000679.1:g.18174710G>A GRCh37
NC_000017.9:g.18115435G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011524001.2:c.*3406C>T XP_011522303.1:n.*3406C>T
XM_024450903.1:c.*3406C>T XP_024306671.1:n.*3406C>T
XR_001752601.2:n.6687C>T