Canonical Allele Identifier: CA382597078

Gene: PPP2R1B

Linked Data

• MyVariant Identifiers: chr11:g.111635575T>A (hg19) ; chr11:g.111764851T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.111764851T>A , CM000673.2:g.111764851T>A	GRCh38
NC_000011.9:g.111635575T>A , CM000673.1:g.111635575T>A	GRCh37
NC_000011.8:g.111140785T>A	NCBI36
NG_012117.1:g.6595A>T
NG_012117.2:g.6595A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000527614.6:c.260A>T MANE Select	ENSP00000437193.1:p.Asn87Ile
ENST00000311129.9:c.260A>T	ENSP00000311344.5:p.Asn87Ile
ENST00000341980.10:c.260A>T	ENSP00000343317.6:p.Asn87Ile
ENST00000393055.6:c.260A>T	ENSP00000376775.2:p.Asn87Ile
ENST00000426998.6:c.114+1397A>T	ENSP00000410671.2:n.114+1397A>T
ENST00000527614.5:c.260A>T	ENSP00000437193.1:p.Asn87Ile
ENST00000531373.1:c.215A>T	ENSP00000434705.1:p.Asn72Ile
ENST00000534500.5:c.205+443A>T	ENSP00000432666.1:n.205+443A>T
ENST00000534521.5:c.260A>T	ENSP00000436626.1:p.Asn87Ile
NM_001177562.1:c.260A>T	NP_001171033.1:p.Asn87Ile
NM_001177563.1:c.260A>T	NP_001171034.1:p.Asn87Ile
NM_002716.4:c.260A>T	NP_002707.3:p.Asn87Ile
NM_181699.2:c.260A>T	NP_859050.1:p.Asn87Ile
NM_181700.1:c.114+1397A>T	NP_859051.1:n.114+1397A>T
XM_006718872.2:c.260A>T	XP_006718935.2:p.Asn87Ile
XM_011542891.1:c.260A>T	XP_011541193.1:p.Asn87Ile
XM_011542892.1:c.260A>T	XP_011541194.1:p.Asn87Ile
XM_011542893.1:c.260A>T	XP_011541195.1:p.Asn87Ile
XR_947857.1:n.288A>T
XM_017017960.2:c.260A>T	XP_016873449.1:p.Asn87Ile
XM_017017961.1:c.260A>T	XP_016873450.1:p.Asn87Ile
XM_024448598.1:c.260A>T	XP_024304366.1:p.Asn87Ile
XM_024448599.1:c.260A>T	XP_024304367.1:p.Asn87Ile
XM_024448600.1:c.260A>T	XP_024304368.1:p.Asn87Ile
NM_001177562.2:c.260A>T	NP_001171033.1:p.Asn87Ile
NM_001177563.2:c.260A>T	NP_001171034.1:p.Asn87Ile
NM_002716.5:c.260A>T MANE Select	NP_002707.3:p.Asn87Ile
NM_181699.3:c.260A>T	NP_859050.1:p.Asn87Ile
NM_181700.2:c.114+1397A>T	NP_859051.1:n.114+1397A>T