Canonical Allele Identifier: CA3492666

Gene: PPP2R2B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.146638334T>C , CM000667.2:g.146638334T>C	GRCh38
NC_000005.9:g.146017897T>C , CM000667.1:g.146017897T>C	GRCh37
NC_000005.8:g.145998090T>C	NCBI36
NG_011570.1:g.448137A>G
NG_011570.2:g.448137A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_181675.4:c.707A>G MANE Select	NP_858061.3:p.Asn236Ser
ENST00000394411.9:c.707A>G MANE Select	ENSP00000377933.3:p.Asn236Ser
NM_001271899.1:c.725A>G	NP_001258828.1:p.Asn242Ser
NM_001271900.1:c.881A>G	NP_001258829.1:p.Asn294Ser
NM_001271900.2:c.881A>G	NP_001258829.1:p.Asn294Ser
NM_001271948.1:c.674A>G	NP_001258877.1:p.Asn225Ser
NM_001271948.2:c.674A>G	NP_001258877.1:p.Asn225Ser
NM_181674.2:c.905A>G	NP_858060.2:p.Asn302Ser
NM_181674.3:c.905A>G	NP_858060.2:p.Asn302Ser
NM_181675.3:c.1025A>G	NP_858061.2:p.Asn342Ser
NM_181676.2:c.716A>G	NP_858062.1:p.Asn239Ser
NM_181676.3:c.716A>G	NP_858062.1:p.Asn239Ser
NM_181677.2:c.647A>G	NP_858063.1:p.Asn216Ser
NM_181678.2:c.674A>G	NP_858064.1:p.Asn225Ser
NR_073526.1:n.1421A>G
NR_073526.2:n.1393A>G
NR_073527.1:n.1058A>G
NR_073527.2:n.888A>G
ENST00000336640.10:c.716A>G	ENSP00000336591.6:p.Asn239Ser
ENST00000394409.7:c.707A>G	ENSP00000377931.4:p.Asn236Ser
ENST00000394411.8:c.707A>G	ENSP00000377933.3:p.Asn236Ser
ENST00000394413.7:c.881A>G	ENSP00000377935.4:p.Asn294Ser
ENST00000394414.5:c.905A>G	ENSP00000377936.1:p.Asn302Ser
ENST00000453001.5:c.674A>G	ENSP00000398779.2:p.Asn225Ser
ENST00000504198.5:c.725A>G	ENSP00000421396.1:p.Asn242Ser
ENST00000508545.6:c.674A>G	ENSP00000431320.1:p.Asn225Ser
ENST00000512639.5:c.*657A>G	ENSP00000426599.1:n.*657A>G
ENST00000530902.5:n.1025A>G