Canonical Allele Identifier: CA805278646
Gene: PPP2R2B HGNC NCBI

Linked Data

dbSNP Id: rs7736604

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146689099G>A , CM000667.2:g.146689099G>A GRCh38
NC_000005.9:g.146068662G>A , CM000667.1:g.146068662G>A GRCh37
NC_000005.8:g.146048855G>A NCBI36
NG_011570.1:g.397372C>T
NG_011570.2:g.397372C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000394411.9:c.447+2029C>T MANE Select ENSP00000377933.3:n.447+2029C>T
ENST00000336640.10:c.456+2029C>T ENSP00000336591.6:n.456+2029C>T
ENST00000394409.7:c.447+2029C>T ENSP00000377931.4:n.447+2029C>T
ENST00000394411.8:c.447+2029C>T ENSP00000377933.3:n.447+2029C>T
ENST00000394413.7:c.621+2029C>T ENSP00000377935.4:n.621+2029C>T
ENST00000394414.5:c.645+2029C>T ENSP00000377936.1:n.645+2029C>T
ENST00000453001.5:c.414+2029C>T ENSP00000398779.2:n.414+2029C>T
ENST00000504198.5:c.465+2029C>T ENSP00000421396.1:n.465+2029C>T
ENST00000508545.6:c.414+2029C>T ENSP00000431320.1:n.414+2029C>T
ENST00000512639.5:c.*397+2029C>T ENSP00000426599.1:n.*397+2029C>T
ENST00000522831.1:n.353-38375C>T
ENST00000530902.5:n.765+2029C>T
NM_001271899.1:c.465+2029C>T NP_001258828.1:n.465+2029C>T
NM_001271900.1:c.621+2029C>T NP_001258829.1:n.621+2029C>T
NM_001271948.1:c.414+2029C>T NP_001258877.1:n.414+2029C>T
NM_181674.2:c.645+2029C>T NP_858060.2:n.645+2029C>T
NM_181675.3:c.765+2029C>T NP_858061.2:n.765+2029C>T
NM_181676.2:c.456+2029C>T NP_858062.1:n.456+2029C>T
NM_181677.2:c.387+2029C>T NP_858063.1:n.387+2029C>T
NM_181678.2:c.414+2029C>T NP_858064.1:n.414+2029C>T
NR_073526.1:n.1161+2029C>T
NR_073527.1:n.798+2029C>T
NM_001271900.2:c.621+2029C>T NP_001258829.1:n.621+2029C>T
NR_073526.2:n.1133+2029C>T
NM_001271948.2:c.414+2029C>T NP_001258877.1:n.414+2029C>T
NM_181674.3:c.645+2029C>T NP_858060.2:n.645+2029C>T
NM_181675.4:c.447+2029C>T MANE Select NP_858061.3:n.447+2029C>T
NM_181676.3:c.456+2029C>T NP_858062.1:n.456+2029C>T
NR_073527.2:n.628+2029C>T