Canonical Allele Identifier: CA382597018

Gene: PPP2R1B

Linked Data

• MyVariant Identifiers: chr11:g.111635566C>A (hg19) ; chr11:g.111764842C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.111764842C>A , CM000673.2:g.111764842C>A	GRCh38
NC_000011.9:g.111635566C>A , CM000673.1:g.111635566C>A	GRCh37
NC_000011.8:g.111140776C>A	NCBI36
NG_012117.1:g.6604G>T
NG_012117.2:g.6604G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000527614.6:c.269G>T MANE Select	ENSP00000437193.1:p.Gly90Val
ENST00000311129.9:c.269G>T	ENSP00000311344.5:p.Gly90Val
ENST00000341980.10:c.269G>T	ENSP00000343317.6:p.Gly90Val
ENST00000393055.6:c.269G>T	ENSP00000376775.2:p.Gly90Val
ENST00000426998.6:c.114+1406G>T	ENSP00000410671.2:n.114+1406G>T
ENST00000527614.5:c.269G>T	ENSP00000437193.1:p.Gly90Val
ENST00000531373.1:c.224G>T	ENSP00000434705.1:p.Gly75Val
ENST00000534500.5:c.205+452G>T	ENSP00000432666.1:n.205+452G>T
ENST00000534521.5:c.269G>T	ENSP00000436626.1:p.Gly90Val
NM_001177562.1:c.269G>T	NP_001171033.1:p.Gly90Val
NM_001177563.1:c.269G>T	NP_001171034.1:p.Gly90Val
NM_002716.4:c.269G>T	NP_002707.3:p.Gly90Val
NM_181699.2:c.269G>T	NP_859050.1:p.Gly90Val
NM_181700.1:c.114+1406G>T	NP_859051.1:n.114+1406G>T
XM_006718872.2:c.269G>T	XP_006718935.2:p.Gly90Val
XM_011542891.1:c.269G>T	XP_011541193.1:p.Gly90Val
XM_011542892.1:c.269G>T	XP_011541194.1:p.Gly90Val
XM_011542893.1:c.269G>T	XP_011541195.1:p.Gly90Val
XR_947857.1:n.297G>T
XM_017017960.2:c.269G>T	XP_016873449.1:p.Gly90Val
XM_017017961.1:c.269G>T	XP_016873450.1:p.Gly90Val
XM_024448598.1:c.269G>T	XP_024304366.1:p.Gly90Val
XM_024448599.1:c.269G>T	XP_024304367.1:p.Gly90Val
XM_024448600.1:c.269G>T	XP_024304368.1:p.Gly90Val
NM_001177562.2:c.269G>T	NP_001171033.1:p.Gly90Val
NM_001177563.2:c.269G>T	NP_001171034.1:p.Gly90Val
NM_002716.5:c.269G>T MANE Select	NP_002707.3:p.Gly90Val
NM_181699.3:c.269G>T	NP_859050.1:p.Gly90Val
NM_181700.2:c.114+1406G>T	NP_859051.1:n.114+1406G>T