Canonical Allele Identifier: CA425499140

Gene: PPP1CB

Linked Data

• MyVariant Identifiers: chr2:g.28999745G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.28776879G>C , CM000664.2:g.28776879G>C	GRCh38
NC_000002.11:g.28999745G>C , CM000664.1:g.28999745G>C	GRCh37
NC_000002.10:g.28853249G>C	NCBI36
NG_052878.1:g.30132G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000418910.2:c.81G>C	ENSP00000388056.2:p.Val27=
ENST00000420282.6:c.81G>C	ENSP00000398839.2:p.Val27=
ENST00000427786.2:c.-4G>C	ENSP00000394589.1:n.-4G>C
ENST00000441461.6:c.81G>C	ENSP00000414918.2:p.Val27=
ENST00000455580.6:c.-4G>C	ENSP00000390715.2:n.-4G>C
ENST00000703171.1:c.81G>C	ENSP00000515217.1:p.Val27=
ENST00000703172.1:c.-4G>C	ENSP00000515218.1:n.-4G>C
ENST00000703173.1:c.81G>C	ENSP00000515219.1:p.Val27=
ENST00000703174.1:c.81G>C	ENSP00000515220.1:p.Val27=
ENST00000703176.1:c.48G>C	ENSP00000515221.1:p.Val16=
ENST00000703177.1:c.-4G>C	ENSP00000515222.1:n.-4G>C
ENST00000395366.3:c.81G>C MANE Select	ENSP00000378769.2:p.Val27=
ENST00000296122.10:c.81G>C	ENSP00000296122.6:p.Val27=
ENST00000358506.6:c.81G>C	ENSP00000351298.2:p.Val27=
ENST00000395366.2:c.81G>C	ENSP00000378769.2:p.Val27=
ENST00000420282.5:c.81G>C	ENSP00000398839.1:p.Val27=
ENST00000427786.1:c.-4G>C	ENSP00000394589.1:n.-4G>C
ENST00000441461.5:c.81G>C	ENSP00000414918.1:p.Val27=
ENST00000455580.5:c.-4G>C	ENSP00000390715.1:n.-4G>C
ENST00000464273.1:n.195G>C
NM_002709.2:c.81G>C	NP_002700.1:p.Val27=
NM_206876.1:c.81G>C	NP_996759.1:p.Val27=
NM_002709.3:c.81G>C MANE Select	NP_002700.1:p.Val27=
NM_206876.2:c.81G>C	NP_996759.1:p.Val27=