Canonical Allele Identifier: CA288434810
Gene: TOP3A HGNC NCBI

Linked Data

dbSNP Id: rs562229174

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18271385A>G , CM000679.2:g.18271385A>G GRCh38
NC_000017.10:g.18174699A>G , CM000679.1:g.18174699A>G GRCh37
NC_000017.9:g.18115424A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011524001.2:c.*3417T>C XP_011522303.1:n.*3417T>C
XM_024450903.1:c.*3417T>C XP_024306671.1:n.*3417T>C
XR_001752601.2:n.6698T>C