Canonical Allele Identifier: CA919802896
Gene: TOP3A HGNC NCBI

Linked Data

dbSNP Id: rs1567728951

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18271385_18271389del , CM000679.2:g.18271385_18271389del GRCh38
NC_000017.10:g.18174699_18174703del , CM000679.1:g.18174699_18174703del GRCh37
NC_000017.9:g.18115424_18115428del NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011524001.2:c.*3415_*3419del XP_011522303.1:n.*3415_*3419del
XM_024450903.1:c.*3415_*3419del XP_024306671.1:n.*3415_*3419del
XR_001752601.2:n.6696_6700del