Canonical Allele Identifier: CA288434739
Gene: TOP3A HGNC NCBI

Linked Data

dbSNP Id: rs10700487

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18271272dup , CM000679.2:g.18271272dup GRCh38
NC_000017.10:g.18174586dup , CM000679.1:g.18174586dup GRCh37
NC_000017.9:g.18115311dup NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011524001.2:c.*3537dup XP_011522303.1:n.*3537dup
XM_024450903.1:c.*3537dup XP_024306671.1:n.*3537dup
XR_001752601.2:n.6818dup