Canonical Allele Identifier: CA2636471254
Gene: TOP3A HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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