Canonical Allele Identifier: CA12088891

Gene: PPP2R2B

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.146845681A>G , CM000667.2:g.146845681A>G	GRCh38
NC_000005.9:g.146225244A>G , CM000667.1:g.146225244A>G	GRCh37
NC_000005.8:g.146205437A>G	NCBI36
NG_011570.1:g.240790T>C
NG_011570.2:g.240790T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394411.9:c.70+32321T>C MANE Select	ENSP00000377933.3:n.70+32321T>C
ENST00000336640.10:c.80-144539T>C	ENSP00000336591.6:n.80-144539T>C
ENST00000394409.7:c.70+32321T>C	ENSP00000377931.4:n.70+32321T>C
ENST00000394411.8:c.70+32321T>C	ENSP00000377933.3:n.70+32321T>C
ENST00000394413.7:c.244+32321T>C	ENSP00000377935.4:n.244+32321T>C
ENST00000394414.5:c.268+32321T>C	ENSP00000377936.1:n.268+32321T>C
ENST00000453001.5:c.37+10818T>C	ENSP00000398779.2:n.37+10818T>C
ENST00000502876.1:n.362+74003T>C
ENST00000504198.5:c.89-144539T>C	ENSP00000421396.1:n.89-144539T>C
ENST00000504565.1:c.*81+32321T>C	ENSP00000425413.1:n.*81+32321T>C
ENST00000508267.5:c.11-144539T>C	ENSP00000421224.1:n.11-144539T>C
ENST00000508545.6:c.37+10818T>C	ENSP00000431320.1:n.37+10818T>C
ENST00000509721.1:n.474+32321T>C
ENST00000512011.5:c.*19-144539T>C	ENSP00000424409.1:n.*19-144539T>C
ENST00000512639.5:c.*20+10818T>C	ENSP00000426599.1:n.*20+10818T>C
ENST00000515880.5:c.*28-144539T>C	ENSP00000421577.1:n.*28-144539T>C
ENST00000520231.1:n.198+76644T>C
ENST00000522831.1:n.352+10818T>C
ENST00000528601.5:c.*20+10818T>C	ENSP00000433890.1:n.*20+10818T>C
ENST00000530902.5:n.388+32321T>C
ENST00000532154.5:c.*20+10818T>C	ENSP00000434497.1:n.*20+10818T>C
NM_001271899.1:c.89-144539T>C	NP_001258828.1:n.89-144539T>C
NM_001271900.1:c.244+32321T>C	NP_001258829.1:n.244+32321T>C
NM_001271948.1:c.37+10818T>C	NP_001258877.1:n.37+10818T>C
NM_181674.2:c.268+32321T>C	NP_858060.2:n.268+32321T>C
NM_181675.3:c.388+32321T>C	NP_858061.2:n.388+32321T>C
NM_181676.2:c.80-144539T>C	NP_858062.1:n.80-144539T>C
NM_181677.2:c.11-144539T>C	NP_858063.1:n.11-144539T>C
NM_181678.2:c.37+10818T>C	NP_858064.1:n.37+10818T>C
NR_073526.1:n.784+32321T>C
NR_073527.1:n.421+32321T>C
NM_001271900.2:c.244+32321T>C	NP_001258829.1:n.244+32321T>C
NR_073526.2:n.756+32321T>C
NM_001271948.2:c.37+10818T>C	NP_001258877.1:n.37+10818T>C
NM_181674.3:c.268+32321T>C	NP_858060.2:n.268+32321T>C
NM_181675.4:c.70+32321T>C MANE Select	NP_858061.3:n.70+32321T>C
NM_181676.3:c.80-144539T>C	NP_858062.1:n.80-144539T>C
NR_073527.2:n.251+32321T>C