Canonical Allele Identifier: CA2287968

Gene: TOP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25598393G>A , CM000665.2:g.25598393G>A	GRCh38
NC_000003.11:g.25639884G>A , CM000665.1:g.25639884G>A	GRCh37
NC_000003.10:g.25614888G>A	NCBI36
NG_029013.1:g.175131G>A
NG_029013.3:g.774071G>A
NG_052961.1:g.70980C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001330700.2:c.4795C>T MANE Select	NP_001317629.1:p.Arg1599Ter
ENST00000264331.9:c.4795C>T MANE Select	ENSP00000264331.4:p.Arg1599Ter
NM_001068.3:c.4780C>T	NP_001059.2:p.Arg1594Ter
NM_001330700.1:c.4795C>T	NP_001317629.1:p.Arg1599Ter
ENST00000264331.8:c.4795C>T	ENSP00000264331.4:p.Arg1599Ter
ENST00000413971.5:c.1640C>T	ENSP00000388216.1:n.1640C>T
ENST00000435706.6:c.4780C>T	ENSP00000396704.2:p.Arg1594Ter
ENST00000470132.2:n.3694C>T
ENST00000699028.1:n.1658C>T
ENST00000699029.1:n.3725C>T
ENST00000699030.1:n.2901C>T
ENST00000699031.1:n.5058C>T
ENST00000699032.1:n.7433C>T
ENST00000699033.1:n.5166C>T
ENST00000699034.1:n.1552C>T
ENST00000699035.1:n.1271C>T
ENST00000699036.1:n.3423C>T
ENST00000699037.1:c.4468C>T	ENSP00000514096.1:p.Arg1490Ter
ENST00000699038.1:c.*2384C>T	ENSP00000514097.1:n.*2384C>T
ENST00000699039.1:n.1461C>T
ENST00000699040.1:n.2265C>T
ENST00000699041.1:n.2976C>T
ENST00000699042.1:n.2334C>T
XM_005265427.2:c.4795C>T	XP_005265484.1:p.Arg1599Ter
XM_011534057.1:c.4684C>T	XP_011532359.1:p.Arg1562Ter
XM_011534057.3:c.4684C>T	XP_011532359.1:p.Arg1562Ter
XR_001740241.2:n.5297C>T