Canonical Allele Identifier: CA346580639

Gene: PPP1CB

Linked Data

• MyVariant Identifiers: chr2:g.28999725T>G (hg19) ; chr2:g.28776859T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.28776859T>G , CM000664.2:g.28776859T>G	GRCh38
NC_000002.11:g.28999725T>G , CM000664.1:g.28999725T>G	GRCh37
NC_000002.10:g.28853229T>G	NCBI36
NG_052878.1:g.30112T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000418910.2:c.61T>G	ENSP00000388056.2:p.Cys21Gly
ENST00000420282.6:c.61T>G	ENSP00000398839.2:p.Cys21Gly
ENST00000427786.2:c.-24T>G	ENSP00000394589.1:n.-24T>G
ENST00000441461.6:c.61T>G	ENSP00000414918.2:p.Cys21Gly
ENST00000455580.6:c.-24T>G	ENSP00000390715.2:n.-24T>G
ENST00000703171.1:c.61T>G	ENSP00000515217.1:p.Cys21Gly
ENST00000703172.1:c.-24T>G	ENSP00000515218.1:n.-24T>G
ENST00000703173.1:c.61T>G	ENSP00000515219.1:p.Cys21Gly
ENST00000703174.1:c.61T>G	ENSP00000515220.1:p.Cys21Gly
ENST00000703176.1:c.28T>G	ENSP00000515221.1:p.Cys10Gly
ENST00000703177.1:c.-24T>G	ENSP00000515222.1:n.-24T>G
ENST00000395366.3:c.61T>G MANE Select	ENSP00000378769.2:p.Cys21Gly
ENST00000296122.10:c.61T>G	ENSP00000296122.6:p.Cys21Gly
ENST00000358506.6:c.61T>G	ENSP00000351298.2:p.Cys21Gly
ENST00000395366.2:c.61T>G	ENSP00000378769.2:p.Cys21Gly
ENST00000420282.5:c.61T>G	ENSP00000398839.1:p.Cys21Gly
ENST00000427786.1:c.-24T>G	ENSP00000394589.1:n.-24T>G
ENST00000441461.5:c.61T>G	ENSP00000414918.1:p.Cys21Gly
ENST00000455580.5:c.-24T>G	ENSP00000390715.1:n.-24T>G
ENST00000464273.1:n.175T>G
NM_002709.2:c.61T>G	NP_002700.1:p.Cys21Gly
NM_206876.1:c.61T>G	NP_996759.1:p.Cys21Gly
NM_002709.3:c.61T>G MANE Select	NP_002700.1:p.Cys21Gly
NM_206876.2:c.61T>G	NP_996759.1:p.Cys21Gly