Canonical Allele Identifier: CA2581503541

Gene: PPP2R2B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.146941260G>C , CM000667.2:g.146941260G>C	GRCh38
NC_000005.9:g.146320823G>C , CM000667.1:g.146320823G>C	GRCh37
NC_000005.8:g.146301016G>C	NCBI36
NG_011570.1:g.145211C>G
NG_011570.2:g.145211C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336640.10:c.79+114405C>G	ENSP00000336591.6:n.79+114405C>G
ENST00000394413.7:c.51-63065C>G	ENSP00000377935.4:n.51-63065C>G
ENST00000394414.5:c.75-63065C>G	ENSP00000377936.1:n.75-63065C>G
ENST00000504198.5:c.88+139799C>G	ENSP00000421396.1:n.88+139799C>G
ENST00000504565.1:c.11-63065C>G	ENSP00000425413.1:n.11-63065C>G
ENST00000508267.5:c.10+93909C>G	ENSP00000421224.1:n.10+93909C>G
ENST00000509721.1:n.281-63065C>G
ENST00000512011.5:c.*18+99457C>G	ENSP00000424409.1:n.*18+99457C>G
ENST00000515880.5:c.*27+113338C>G	ENSP00000421577.1:n.*27+113338C>G
ENST00000522831.1:n.268-84677C>G
NM_001271899.1:c.88+139799C>G	NP_001258828.1:n.88+139799C>G
NM_001271900.1:c.51-63065C>G	NP_001258829.1:n.51-63065C>G
NM_181674.2:c.75-63065C>G	NP_858060.2:n.75-63065C>G
NM_181676.2:c.79+114405C>G	NP_858062.1:n.79+114405C>G
NM_181677.2:c.10+93909C>G	NP_858063.1:n.10+93909C>G
NM_181678.2:c.-48-84677C>G	NP_858064.1:n.-48-84677C>G
NM_001271900.2:c.51-63065C>G	NP_001258829.1:n.51-63065C>G
NM_181674.3:c.75-63065C>G	NP_858060.2:n.75-63065C>G
NM_181676.3:c.79+114405C>G	NP_858062.1:n.79+114405C>G