Canonical Allele Identifier: CA982006314
Gene: TOP3A HGNC NCBI

Linked Data

dbSNP Id: rs1978977062

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18271269G>A , CM000679.2:g.18271269G>A GRCh38
NC_000017.10:g.18174583G>A , CM000679.1:g.18174583G>A GRCh37
NC_000017.9:g.18115308G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011524001.2:c.*3533C>T XP_011522303.1:n.*3533C>T
XM_024450903.1:c.*3533C>T XP_024306671.1:n.*3533C>T
XR_001752601.2:n.6814C>T