Canonical Allele Identifier: CA3131044135

Gene: PPP2R2B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.146958316C>G , CM000667.2:g.146958316C>G	GRCh38
NC_000005.9:g.146337879C>G , CM000667.1:g.146337879C>G	GRCh37
NC_000005.8:g.146318072C>G	NCBI36
NG_011570.1:g.128155G>C
NG_011570.2:g.128155G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001271899.1:c.88+122743G>C	NP_001258828.1:n.88+122743G>C
NM_001271900.1:c.51-80121G>C	NP_001258829.1:n.51-80121G>C
NM_001271900.2:c.51-80121G>C	NP_001258829.1:n.51-80121G>C
NM_181674.2:c.75-80121G>C	NP_858060.2:n.75-80121G>C
NM_181674.3:c.75-80121G>C	NP_858060.2:n.75-80121G>C
NM_181676.2:c.79+97349G>C	NP_858062.1:n.79+97349G>C
NM_181676.3:c.79+97349G>C	NP_858062.1:n.79+97349G>C
NM_181677.2:c.10+76853G>C	NP_858063.1:n.10+76853G>C
NM_181678.2:c.-48-101733G>C	NP_858064.1:n.-48-101733G>C
ENST00000336640.10:c.79+97349G>C	ENSP00000336591.6:n.79+97349G>C
ENST00000394413.7:c.51-80121G>C	ENSP00000377935.4:n.51-80121G>C
ENST00000394414.5:c.75-80121G>C	ENSP00000377936.1:n.75-80121G>C
ENST00000504198.5:c.88+122743G>C	ENSP00000421396.1:n.88+122743G>C
ENST00000504565.1:c.10+76853G>C	ENSP00000425413.1:n.10+76853G>C
ENST00000508267.5:c.10+76853G>C	ENSP00000421224.1:n.10+76853G>C
ENST00000509721.1:n.281-80121G>C
ENST00000512011.5:c.*18+82401G>C	ENSP00000424409.1:n.*18+82401G>C
ENST00000515880.5:c.*27+96282G>C	ENSP00000421577.1:n.*27+96282G>C
ENST00000522831.1:n.267+97349G>C