Canonical Allele Identifier: CA10414753

Gene: CCNB3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50311170G>C , CM000685.2:g.50311170G>C	GRCh38
NC_000023.10:g.50054170G>C , CM000685.1:g.50054170G>C	GRCh37
NC_000023.9:g.50070910G>C	NCBI36
NG_012880.1:g.29997G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376042.6:c.3001G>C MANE Select	ENSP00000365210.1:p.Gly1001Arg
ENST00000276014.11:c.3001G>C	ENSP00000276014.7:p.Gly1001Arg
ENST00000348603.2:c.204+22283G>C	ENSP00000338682.2:n.204+22283G>C
ENST00000376038.5:c.204+22283G>C	ENSP00000365206.1:n.204+22283G>C
ENST00000376042.5:c.3001G>C	ENSP00000365210.1:p.Gly1001Arg
ENST00000476167.5:c.336-1367G>C	ENSP00000431645.1:n.336-1367G>C
NM_033031.2:c.3001G>C	NP_149020.2:p.Gly1001Arg
NM_033670.2:c.204+22283G>C	NP_391990.1:n.204+22283G>C
XM_006724610.2:c.3001G>C	XP_006724673.1:p.Gly1001Arg
XM_011530832.1:c.3001G>C	XP_011529134.1:p.Gly1001Arg
XM_011530833.1:c.2824-69G>C	XP_011529135.1:n.2824-69G>C
XM_017029913.1:c.3001G>C	XP_016885402.1:p.Gly1001Arg
XM_017029914.1:c.3001G>C	XP_016885403.1:p.Gly1001Arg
XM_017029915.1:c.3001G>C	XP_016885404.1:p.Gly1001Arg
XM_017029916.1:c.3001G>C	XP_016885405.1:p.Gly1001Arg
XM_017029917.1:c.3001G>C	XP_016885406.1:p.Gly1001Arg
XM_017029918.1:c.3001G>C	XP_016885407.1:p.Gly1001Arg
XM_024452472.1:c.3001G>C	XP_024308240.1:p.Gly1001Arg
NM_033031.3:c.3001G>C MANE Select	NP_149020.2:p.Gly1001Arg
NM_033670.3:c.204+22283G>C	NP_391990.1:n.204+22283G>C
NM_033670.4:c.204+22283G>C	NP_391990.1:n.204+22283G>C