Canonical Allele Identifier: CA10414666

Gene: CCNB3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50310275C>T , CM000685.2:g.50310275C>T	GRCh38
NC_000023.10:g.50053275C>T , CM000685.1:g.50053275C>T	GRCh37
NC_000023.9:g.50070015C>T	NCBI36
NG_012880.1:g.29102C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376042.6:c.2106C>T MANE Select	ENSP00000365210.1:p.Ala702=
ENST00000276014.11:c.2106C>T	ENSP00000276014.7:p.Ala702=
ENST00000348603.2:c.204+21388C>T	ENSP00000338682.2:n.204+21388C>T
ENST00000376038.5:c.204+21388C>T	ENSP00000365206.1:n.204+21388C>T
ENST00000376042.5:c.2106C>T	ENSP00000365210.1:p.Ala702=
ENST00000476167.5:c.336-2262C>T	ENSP00000431645.1:n.336-2262C>T
NM_033031.2:c.2106C>T	NP_149020.2:p.Ala702=
NM_033670.2:c.204+21388C>T	NP_391990.1:n.204+21388C>T
XM_006724610.2:c.2106C>T	XP_006724673.1:p.Ala702=
XM_011530832.1:c.2106C>T	XP_011529134.1:p.Ala702=
XM_011530833.1:c.2106C>T	XP_011529135.1:p.Ala702=
XM_017029913.1:c.2106C>T	XP_016885402.1:p.Ala702=
XM_017029914.1:c.2106C>T	XP_016885403.1:p.Ala702=
XM_017029915.1:c.2106C>T	XP_016885404.1:p.Ala702=
XM_017029916.1:c.2106C>T	XP_016885405.1:p.Ala702=
XM_017029917.1:c.2106C>T	XP_016885406.1:p.Ala702=
XM_017029918.1:c.2106C>T	XP_016885407.1:p.Ala702=
XM_024452472.1:c.2106C>T	XP_024308240.1:p.Ala702=
NM_033031.3:c.2106C>T MANE Select	NP_149020.2:p.Ala702=
NM_033670.3:c.204+21388C>T	NP_391990.1:n.204+21388C>T
NM_033670.4:c.204+21388C>T	NP_391990.1:n.204+21388C>T