Canonical Allele Identifier: CA2288028

Gene: TOP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25599498T>C , CM000665.2:g.25599498T>C	GRCh38
NC_000003.11:g.25640989T>C , CM000665.1:g.25640989T>C	GRCh37
NC_000003.10:g.25615993T>C	NCBI36
NG_029013.1:g.176236T>C
NG_029013.3:g.775176T>C
NG_052961.1:g.69875A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001330700.2:c.4647A>G MANE Select	NP_001317629.1:p.Ala1549=
ENST00000264331.9:c.4647A>G MANE Select	ENSP00000264331.4:p.Ala1549=
NM_001068.3:c.4632A>G	NP_001059.2:p.Ala1544=
NM_001330700.1:c.4647A>G	NP_001317629.1:p.Ala1549=
ENST00000264331.8:c.4647A>G	ENSP00000264331.4:p.Ala1549=
ENST00000413971.5:c.1492A>G	ENSP00000388216.1:n.1492A>G
ENST00000435706.6:c.4632A>G	ENSP00000396704.2:p.Ala1544=
ENST00000470132.2:n.3546A>G
ENST00000699028.1:n.1510A>G
ENST00000699029.1:n.3577A>G
ENST00000699030.1:n.2753A>G
ENST00000699031.1:n.4910A>G
ENST00000699032.1:n.7285A>G
ENST00000699033.1:n.5018A>G
ENST00000699034.1:n.447A>G
ENST00000699035.1:n.1123A>G
ENST00000699036.1:n.3275A>G
ENST00000699037.1:c.4320A>G	ENSP00000514096.1:p.Ala1440=
ENST00000699038.1:c.*1279A>G	ENSP00000514097.1:n.*1279A>G
ENST00000699039.1:n.1313A>G
ENST00000699040.1:n.1160A>G
ENST00000699041.1:n.2828A>G
ENST00000699042.1:n.2186A>G
XM_005265427.2:c.4647A>G	XP_005265484.1:p.Ala1549=
XM_011534057.1:c.4536A>G	XP_011532359.1:p.Ala1512=
XM_011534057.3:c.4536A>G	XP_011532359.1:p.Ala1512=
XR_001740241.2:n.5149A>G