Canonical Allele Identifier: CA2636471290
Gene: TOP3A HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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