Canonical Allele Identifier: CA2636471252
Gene: TOP3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18271376C>A , CM000679.2:g.18271376C>A GRCh38
NC_000017.10:g.18174690C>A , CM000679.1:g.18174690C>A GRCh37
NC_000017.9:g.18115415C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011524001.2:c.*3426G>T XP_011522303.1:n.*3426G>T
XM_024450903.1:c.*3426G>T XP_024306671.1:n.*3426G>T
XR_001752601.2:n.6707G>T