Canonical Allele Identifier: CA726686573
Gene: TOP3A HGNC NCBI

Linked Data

dbSNP Id: rs1481578394

Genomic Alleles

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

Transcript Alleles

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