Canonical Allele Identifier: CA15372917

Gene: PPP2R2B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.147035653C>T , CM000667.2:g.147035653C>T	GRCh38
NC_000005.9:g.146415216C>T , CM000667.1:g.146415216C>T	GRCh37
NC_000005.8:g.146395409C>T	NCBI36
NG_011570.1:g.50818G>A
NG_011570.2:g.50818G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336640.10:c.79+20012G>A	ENSP00000336591.6:n.79+20012G>A
ENST00000394413.7:c.50+45406G>A	ENSP00000377935.4:n.50+45406G>A
ENST00000394414.5:c.74+20012G>A	ENSP00000377936.1:n.74+20012G>A
ENST00000504198.5:c.88+45406G>A	ENSP00000421396.1:n.88+45406G>A
ENST00000504565.1:c.-62-413G>A	ENSP00000425413.1:n.-62-413G>A
ENST00000508267.5:c.-62-413G>A	ENSP00000421224.1:n.-62-413G>A
ENST00000509721.1:n.280+45406G>A
ENST00000512011.5:c.*18+5064G>A	ENSP00000424409.1:n.*18+5064G>A
ENST00000515880.5:c.*27+18945G>A	ENSP00000421577.1:n.*27+18945G>A
ENST00000522831.1:n.267+20012G>A
NM_001271899.1:c.88+45406G>A	NP_001258828.1:n.88+45406G>A
NM_001271900.1:c.50+45406G>A	NP_001258829.1:n.50+45406G>A
NM_181674.2:c.74+20012G>A	NP_858060.2:n.74+20012G>A
NM_181676.2:c.79+20012G>A	NP_858062.1:n.79+20012G>A
NM_181677.2:c.-62-413G>A	NP_858063.1:n.-62-413G>A
NM_181678.2:c.-49+45406G>A	NP_858064.1:n.-49+45406G>A
NM_001271900.2:c.50+45406G>A	NP_001258829.1:n.50+45406G>A
NM_181674.3:c.74+20012G>A	NP_858060.2:n.74+20012G>A
NM_181676.3:c.79+20012G>A	NP_858062.1:n.79+20012G>A