Canonical Allele Identifier: CA432842371

Gene: TOP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25638280A>G , CM000665.2:g.25638280A>G	GRCh38
NC_000003.11:g.25679771A>G , CM000665.1:g.25679771A>G	GRCh37
NC_000003.10:g.25654775A>G	NCBI36
NG_052961.1:g.31093T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001330700.2:c.426T>C MANE Select	NP_001317629.1:p.Asn142=
ENST00000264331.9:c.426T>C MANE Select	ENSP00000264331.4:p.Asn142=
NM_001068.3:c.411T>C	NP_001059.2:p.Asn137=
NM_001330700.1:c.426T>C	NP_001317629.1:p.Asn142=
ENST00000264331.8:c.426T>C	ENSP00000264331.4:p.Asn142=
ENST00000424225.1:c.411T>C	ENSP00000391112.1:p.Asn137=
ENST00000435706.6:c.411T>C	ENSP00000396704.2:p.Asn137=
ENST00000699031.1:n.270T>C
ENST00000699032.1:n.270T>C
ENST00000699033.1:n.270T>C
ENST00000699037.1:c.183T>C	ENSP00000514096.1:p.Asn61=
ENST00000699038.1:c.183T>C	ENSP00000514097.1:p.Asn61=
ENST00000699043.1:c.183T>C	ENSP00000514098.1:p.Asn61=
ENST00000699044.1:n.270T>C
XM_005265427.2:c.426T>C	XP_005265484.1:p.Asn142=
XM_011534057.1:c.426T>C	XP_011532359.1:p.Asn142=
XM_011534057.3:c.426T>C	XP_011532359.1:p.Asn142=
XR_001740241.2:n.1020T>C
XR_940497.1:n.1034T>C