Canonical Allele Identifier: CA2000412497

Gene: PPP2R1B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.111764852T= , CM000673.2:g.111764852T=	GRCh38
NC_000011.9:g.111635576T= , CM000673.1:g.111635576T=	GRCh37
NC_000011.8:g.111140786T=	NCBI36
NG_012117.1:g.6594A=
NG_012117.2:g.6594A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000527614.6:c.259A= MANE Select	ENSP00000437193.1:p.Asn87=
ENST00000311129.9:c.259A=	ENSP00000311344.5:p.Asn87=
ENST00000341980.10:c.259A=	ENSP00000343317.6:p.Asn87=
ENST00000393055.6:c.259A=	ENSP00000376775.2:p.Asn87=
ENST00000426998.6:c.114+1396A=	ENSP00000410671.2:n.114+1396A=
ENST00000527614.5:c.259A=	ENSP00000437193.1:p.Asn87=
ENST00000531373.1:c.214A=	ENSP00000434705.1:p.Asn72=
ENST00000534500.5:c.205+442A=	ENSP00000432666.1:n.205+442A=
ENST00000534521.5:c.259A=	ENSP00000436626.1:p.Asn87=
NM_001177562.1:c.259A=	NP_001171033.1:p.Asn87=
NM_001177563.1:c.259A=	NP_001171034.1:p.Asn87=
NM_002716.4:c.259A=	NP_002707.3:p.Asn87=
NM_181699.2:c.259A=	NP_859050.1:p.Asn87=
NM_181700.1:c.114+1396A=	NP_859051.1:n.114+1396A=
XM_006718872.2:c.259A=	XP_006718935.2:p.Asn87=
XM_011542891.1:c.259A=	XP_011541193.1:p.Asn87=
XM_011542892.1:c.259A=	XP_011541194.1:p.Asn87=
XM_011542893.1:c.259A=	XP_011541195.1:p.Asn87=
XR_947857.1:n.287A=
XM_017017960.2:c.259A=	XP_016873449.1:p.Asn87=
XM_017017961.1:c.259A=	XP_016873450.1:p.Asn87=
XM_024448598.1:c.259A=	XP_024304366.1:p.Asn87=
XM_024448599.1:c.259A=	XP_024304367.1:p.Asn87=
XM_024448600.1:c.259A=	XP_024304368.1:p.Asn87=
NM_001177562.2:c.259A=	NP_001171033.1:p.Asn87=
NM_001177563.2:c.259A=	NP_001171034.1:p.Asn87=
NM_002716.5:c.259A= MANE Select	NP_002707.3:p.Asn87=
NM_181699.3:c.259A=	NP_859050.1:p.Asn87=
NM_181700.2:c.114+1396A=	NP_859051.1:n.114+1396A=