Canonical Allele Identifier: CA2739312569
Gene: TOP3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18271367G>T , CM000679.2:g.18271367G>T GRCh38
NC_000017.10:g.18174681G>T , CM000679.1:g.18174681G>T GRCh37
NC_000017.9:g.18115406G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011524001.2:c.*3435C>A XP_011522303.1:n.*3435C>A
XM_024450903.1:c.*3435C>A XP_024306671.1:n.*3435C>A
XR_001752601.2:n.6716C>A