Canonical Allele Identifier: CA382597068

Gene: PPP2R1B

Linked Data

• MyVariant Identifiers: chr11:g.111635573A>C (hg19) ; chr11:g.111764849A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.111764849A>C , CM000673.2:g.111764849A>C	GRCh38
NC_000011.9:g.111635573A>C , CM000673.1:g.111635573A>C	GRCh37
NC_000011.8:g.111140783A>C	NCBI36
NG_012117.1:g.6597T>G
NG_012117.2:g.6597T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000527614.6:c.262T>G MANE Select	ENSP00000437193.1:p.Phe88Val
ENST00000311129.9:c.262T>G	ENSP00000311344.5:p.Phe88Val
ENST00000341980.10:c.262T>G	ENSP00000343317.6:p.Phe88Val
ENST00000393055.6:c.262T>G	ENSP00000376775.2:p.Phe88Val
ENST00000426998.6:c.114+1399T>G	ENSP00000410671.2:n.114+1399T>G
ENST00000527614.5:c.262T>G	ENSP00000437193.1:p.Phe88Val
ENST00000531373.1:c.217T>G	ENSP00000434705.1:p.Phe73Val
ENST00000534500.5:c.205+445T>G	ENSP00000432666.1:n.205+445T>G
ENST00000534521.5:c.262T>G	ENSP00000436626.1:p.Phe88Val
NM_001177562.1:c.262T>G	NP_001171033.1:p.Phe88Val
NM_001177563.1:c.262T>G	NP_001171034.1:p.Phe88Val
NM_002716.4:c.262T>G	NP_002707.3:p.Phe88Val
NM_181699.2:c.262T>G	NP_859050.1:p.Phe88Val
NM_181700.1:c.114+1399T>G	NP_859051.1:n.114+1399T>G
XM_006718872.2:c.262T>G	XP_006718935.2:p.Phe88Val
XM_011542891.1:c.262T>G	XP_011541193.1:p.Phe88Val
XM_011542892.1:c.262T>G	XP_011541194.1:p.Phe88Val
XM_011542893.1:c.262T>G	XP_011541195.1:p.Phe88Val
XR_947857.1:n.290T>G
XM_017017960.2:c.262T>G	XP_016873449.1:p.Phe88Val
XM_017017961.1:c.262T>G	XP_016873450.1:p.Phe88Val
XM_024448598.1:c.262T>G	XP_024304366.1:p.Phe88Val
XM_024448599.1:c.262T>G	XP_024304367.1:p.Phe88Val
XM_024448600.1:c.262T>G	XP_024304368.1:p.Phe88Val
NM_001177562.2:c.262T>G	NP_001171033.1:p.Phe88Val
NM_001177563.2:c.262T>G	NP_001171034.1:p.Phe88Val
NM_002716.5:c.262T>G MANE Select	NP_002707.3:p.Phe88Val
NM_181699.3:c.262T>G	NP_859050.1:p.Phe88Val
NM_181700.2:c.114+1399T>G	NP_859051.1:n.114+1399T>G