Canonical Allele Identifier: CA10414547

Gene: CCNB3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50309002T>C , CM000685.2:g.50309002T>C	GRCh38
NC_000023.10:g.50052002T>C , CM000685.1:g.50052002T>C	GRCh37
NC_000023.9:g.50068742T>C	NCBI36
NG_012880.1:g.27829T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_033031.3:c.833T>C MANE Select	NP_149020.2:p.Ile278Thr
ENST00000376042.6:c.833T>C MANE Select	ENSP00000365210.1:p.Ile278Thr
NM_033031.2:c.833T>C	NP_149020.2:p.Ile278Thr
NM_033670.2:c.204+20115T>C	NP_391990.1:n.204+20115T>C
NM_033670.3:c.204+20115T>C	NP_391990.1:n.204+20115T>C
NM_033670.4:c.204+20115T>C	NP_391990.1:n.204+20115T>C
ENST00000276014.11:c.833T>C	ENSP00000276014.7:p.Ile278Thr
ENST00000348603.2:c.204+20115T>C	ENSP00000338682.2:n.204+20115T>C
ENST00000376038.5:c.204+20115T>C	ENSP00000365206.1:n.204+20115T>C
ENST00000376042.5:c.833T>C	ENSP00000365210.1:p.Ile278Thr
ENST00000476167.5:c.336-3535T>C	ENSP00000431645.1:n.336-3535T>C
XM_006724610.2:c.833T>C	XP_006724673.1:p.Ile278Thr
XM_011530832.1:c.833T>C	XP_011529134.1:p.Ile278Thr
XM_011530833.1:c.833T>C	XP_011529135.1:p.Ile278Thr
XM_017029913.1:c.833T>C	XP_016885402.1:p.Ile278Thr
XM_017029914.1:c.833T>C	XP_016885403.1:p.Ile278Thr
XM_017029915.1:c.833T>C	XP_016885404.1:p.Ile278Thr
XM_017029916.1:c.833T>C	XP_016885405.1:p.Ile278Thr
XM_017029917.1:c.833T>C	XP_016885406.1:p.Ile278Thr
XM_017029918.1:c.833T>C	XP_016885407.1:p.Ile278Thr
XM_024452472.1:c.833T>C	XP_024308240.1:p.Ile278Thr