Canonical Allele Identifier: CA726686505
Gene: TOP3A HGNC NCBI

Linked Data

dbSNP Id: rs10700487

Genomic Alleles

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

Transcript Alleles

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