Canonical Allele Identifier: CA2250914952
Gene: TOP3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18271381T= , CM000679.2:g.18271381T= GRCh38
NC_000017.10:g.18174695T= , CM000679.1:g.18174695T= GRCh37
NC_000017.9:g.18115420T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011524001.2:c.*3421A= XP_011522303.1:n.*3421A=
XM_024450903.1:c.*3421A= XP_024306671.1:n.*3421A=
XR_001752601.2:n.6702A=