Canonical Allele Identifier: CA2636471238
Gene: TOP3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18271369T>A , CM000679.2:g.18271369T>A GRCh38
NC_000017.10:g.18174683T>A , CM000679.1:g.18174683T>A GRCh37
NC_000017.9:g.18115408T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011524001.2:c.*3433A>T XP_011522303.1:n.*3433A>T
XM_024450903.1:c.*3433A>T XP_024306671.1:n.*3433A>T
XR_001752601.2:n.6714A>T