Canonical Allele Identifier: CA346580634
Gene: PPP1CB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.28776857G>A , CM000664.2:g.28776857G>A GRCh38
NC_000002.11:g.28999723G>A , CM000664.1:g.28999723G>A GRCh37
NC_000002.10:g.28853227G>A NCBI36
NG_052878.1:g.30110G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000418910.2:c.59G>A ENSP00000388056.2:p.Gly20Glu
ENST00000420282.6:c.59G>A ENSP00000398839.2:p.Gly20Glu
ENST00000427786.2:c.-26G>A ENSP00000394589.1:n.-26G>A
ENST00000441461.6:c.59G>A ENSP00000414918.2:p.Gly20Glu
ENST00000455580.6:c.-26G>A ENSP00000390715.2:n.-26G>A
ENST00000703171.1:c.59G>A ENSP00000515217.1:p.Gly20Glu
ENST00000703172.1:c.-26G>A ENSP00000515218.1:n.-26G>A
ENST00000703173.1:c.59G>A ENSP00000515219.1:p.Gly20Glu
ENST00000703174.1:c.59G>A ENSP00000515220.1:p.Gly20Glu
ENST00000703176.1:c.26G>A ENSP00000515221.1:p.Gly9Glu
ENST00000703177.1:c.-26G>A ENSP00000515222.1:n.-26G>A
ENST00000395366.3:c.59G>A MANE Select ENSP00000378769.2:p.Gly20Glu
ENST00000296122.10:c.59G>A ENSP00000296122.6:p.Gly20Glu
ENST00000358506.6:c.59G>A ENSP00000351298.2:p.Gly20Glu
ENST00000395366.2:c.59G>A ENSP00000378769.2:p.Gly20Glu
ENST00000420282.5:c.59G>A ENSP00000398839.1:p.Gly20Glu
ENST00000427786.1:c.-26G>A ENSP00000394589.1:n.-26G>A
ENST00000441461.5:c.59G>A ENSP00000414918.1:p.Gly20Glu
ENST00000455580.5:c.-26G>A ENSP00000390715.1:n.-26G>A
ENST00000464273.1:n.173G>A
NM_002709.2:c.59G>A NP_002700.1:p.Gly20Glu
NM_206876.1:c.59G>A NP_996759.1:p.Gly20Glu
NM_002709.3:c.59G>A MANE Select NP_002700.1:p.Gly20Glu
NM_206876.2:c.59G>A NP_996759.1:p.Gly20Glu