Canonical Allele Identifier: CA1240875807

Gene: PPP1CB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.28776854G= , CM000664.2:g.28776854G=	GRCh38
NC_000002.11:g.28999720G= , CM000664.1:g.28999720G=	GRCh37
NC_000002.10:g.28853224G=	NCBI36
NG_052878.1:g.30107G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000418910.2:c.56G=	ENSP00000388056.2:p.Arg19=
ENST00000420282.6:c.56G=	ENSP00000398839.2:p.Arg19=
ENST00000427786.2:c.-29G=	ENSP00000394589.1:n.-29G=
ENST00000441461.6:c.56G=	ENSP00000414918.2:p.Arg19=
ENST00000455580.6:c.-29G=	ENSP00000390715.2:n.-29G=
ENST00000703171.1:c.56G=	ENSP00000515217.1:p.Arg19=
ENST00000703172.1:c.-29G=	ENSP00000515218.1:n.-29G=
ENST00000703173.1:c.56G=	ENSP00000515219.1:p.Arg19=
ENST00000703174.1:c.56G=	ENSP00000515220.1:p.Arg19=
ENST00000703176.1:c.23G=	ENSP00000515221.1:p.Arg8=
ENST00000703177.1:c.-29G=	ENSP00000515222.1:n.-29G=
ENST00000395366.3:c.56G= MANE Select	ENSP00000378769.2:p.Arg19=
ENST00000296122.10:c.56G=	ENSP00000296122.6:p.Arg19=
ENST00000358506.6:c.56G=	ENSP00000351298.2:p.Arg19=
ENST00000395366.2:c.56G=	ENSP00000378769.2:p.Arg19=
ENST00000420282.5:c.56G=	ENSP00000398839.1:p.Arg19=
ENST00000427786.1:c.-29G=	ENSP00000394589.1:n.-29G=
ENST00000441461.5:c.56G=	ENSP00000414918.1:p.Arg19=
ENST00000455580.5:c.-29G=	ENSP00000390715.1:n.-29G=
ENST00000464273.1:n.170G=
NM_002709.2:c.56G=	NP_002700.1:p.Arg19=
NM_206876.1:c.56G=	NP_996759.1:p.Arg19=
NM_002709.3:c.56G= MANE Select	NP_002700.1:p.Arg19=
NM_206876.2:c.56G=	NP_996759.1:p.Arg19=