Canonical Allele Identifier: CA351910786

Gene: TOP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25632745A>T , CM000665.2:g.25632745A>T	GRCh38
NC_000003.11:g.25674236A>T , CM000665.1:g.25674236A>T	GRCh37
NC_000003.10:g.25649240A>T	NCBI36
NG_052961.1:g.36628T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699031.1:n.920T>A
ENST00000699032.1:n.920T>A
ENST00000699033.1:n.920T>A
ENST00000699037.1:c.833T>A	ENSP00000514096.1:p.Ile278Asn
ENST00000699038.1:c.833T>A	ENSP00000514097.1:p.Ile278Asn
ENST00000699043.1:c.833T>A	ENSP00000514098.1:p.Ile278Asn
ENST00000699044.1:n.920T>A
ENST00000264331.9:c.1076T>A MANE Select	ENSP00000264331.4:p.Ile359Asn
ENST00000264331.8:c.1076T>A	ENSP00000264331.4:p.Ile359Asn
ENST00000424225.1:c.1061T>A	ENSP00000391112.1:p.Ile354Asn
ENST00000435706.6:c.1061T>A	ENSP00000396704.2:p.Ile354Asn
NM_001068.3:c.1061T>A	NP_001059.2:p.Ile354Asn
XM_005265427.2:c.1076T>A	XP_005265484.1:p.Ile359Asn
XM_011534057.1:c.1076T>A	XP_011532359.1:p.Ile359Asn
XR_940497.1:n.1684T>A
NM_001330700.1:c.1076T>A	NP_001317629.1:p.Ile359Asn
XM_011534057.3:c.1076T>A	XP_011532359.1:p.Ile359Asn
XR_001740241.2:n.1670T>A
NM_001330700.2:c.1076T>A MANE Select	NP_001317629.1:p.Ile359Asn