Canonical Allele Identifier: CA2000412446

Gene: PPP2R1B

Linked Data

• dbSNP Id: rs782685052
• gnomAD v4: 11-111764765-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.111764765A>G , CM000673.2:g.111764765A>G	GRCh38
NC_000011.9:g.111635489A>G , CM000673.1:g.111635489A>G	GRCh37
NC_000011.8:g.111140699A>G	NCBI36
NG_012117.1:g.6681T>C
NG_012117.2:g.6681T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000527614.6:c.306+40T>C MANE Select	ENSP00000437193.1:n.306+40T>C
ENST00000311129.9:c.306+40T>C	ENSP00000311344.5:n.306+40T>C
ENST00000341980.10:c.306+40T>C	ENSP00000343317.6:n.306+40T>C
ENST00000393055.6:c.306+40T>C	ENSP00000376775.2:n.306+40T>C
ENST00000426998.6:c.114+1483T>C	ENSP00000410671.2:n.114+1483T>C
ENST00000527614.5:c.306+40T>C	ENSP00000437193.1:n.306+40T>C
ENST00000531373.1:c.261+40T>C	ENSP00000434705.1:n.261+40T>C
ENST00000534500.5:c.205+529T>C	ENSP00000432666.1:n.205+529T>C
ENST00000534521.5:c.306+40T>C	ENSP00000436626.1:n.306+40T>C
NM_001177562.1:c.306+40T>C	NP_001171033.1:n.306+40T>C
NM_001177563.1:c.306+40T>C	NP_001171034.1:n.306+40T>C
NM_002716.4:c.306+40T>C	NP_002707.3:n.306+40T>C
NM_181699.2:c.306+40T>C	NP_859050.1:n.306+40T>C
NM_181700.1:c.114+1483T>C	NP_859051.1:n.114+1483T>C
XM_006718872.2:c.306+40T>C	XP_006718935.2:n.306+40T>C
XM_011542891.1:c.306+40T>C	XP_011541193.1:n.306+40T>C
XM_011542892.1:c.306+40T>C	XP_011541194.1:n.306+40T>C
XM_011542893.1:c.306+40T>C	XP_011541195.1:n.306+40T>C
XR_947857.1:n.334+40T>C
XM_017017960.2:c.306+40T>C	XP_016873449.1:n.306+40T>C
XM_017017961.1:c.306+40T>C	XP_016873450.1:n.306+40T>C
XM_024448598.1:c.306+40T>C	XP_024304366.1:n.306+40T>C
XM_024448599.1:c.306+40T>C	XP_024304367.1:n.306+40T>C
XM_024448600.1:c.306+40T>C	XP_024304368.1:n.306+40T>C
NM_001177562.2:c.306+40T>C	NP_001171033.1:n.306+40T>C
NM_001177563.2:c.306+40T>C	NP_001171034.1:n.306+40T>C
NM_002716.5:c.306+40T>C MANE Select	NP_002707.3:n.306+40T>C
NM_181699.3:c.306+40T>C	NP_859050.1:n.306+40T>C
NM_181700.2:c.114+1483T>C	NP_859051.1:n.114+1483T>C