Canonical Allele Identifier: CA10588830

Gene: TOP2B

Linked Data

• ClinVar Variation Id: 265791
• ClinVar RCV Id: RCV000256202
• dbSNP Id: rs886039770
• MyVariant Identifiers: chr3:g.25686844G>A (hg19) ; chr3:g.25645353G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25645353G>A , CM000665.2:g.25645353G>A	GRCh38
NC_000003.11:g.25686844G>A , CM000665.1:g.25686844G>A	GRCh37
NC_000003.10:g.25661848G>A	NCBI36
NG_052961.1:g.24020C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699031.1:n.31C>T
ENST00000699032.1:n.31C>T
ENST00000699033.1:n.31C>T
ENST00000699037.1:c.-57C>T	ENSP00000514096.1:n.-57C>T
ENST00000699038.1:c.-57C>T	ENSP00000514097.1:n.-57C>T
ENST00000699043.1:c.-57C>T	ENSP00000514098.1:n.-57C>T
ENST00000699044.1:n.31C>T
ENST00000264331.9:c.187C>T MANE Select	ENSP00000264331.4:p.His63Tyr
ENST00000264331.8:c.187C>T	ENSP00000264331.4:p.His63Tyr
ENST00000424225.1:c.172C>T	ENSP00000391112.1:p.His58Tyr
ENST00000435706.6:c.172C>T	ENSP00000396704.2:p.His58Tyr
NM_001068.3:c.172C>T	NP_001059.2:p.His58Tyr
XM_005265427.2:c.187C>T	XP_005265484.1:p.His63Tyr
XM_011534057.1:c.187C>T	XP_011532359.1:p.His63Tyr
XR_940497.1:n.795C>T
NM_001330700.1:c.187C>T	NP_001317629.1:p.His63Tyr
XM_011534057.3:c.187C>T	XP_011532359.1:p.His63Tyr
XR_001740241.2:n.781C>T
NM_001330700.2:c.187C>T MANE Select	NP_001317629.1:p.His63Tyr