Canonical Allele Identifier: CA2686824438

Gene: PPP2CB

Linked Data

• gnomAD v4: 8-30786113-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.30786113C>A , CM000670.2:g.30786113C>A	GRCh38
NC_000008.10:g.30643629C>A , CM000670.1:g.30643629C>A	GRCh37
NC_000008.9:g.30763171C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000221138.9:c.*122G>T MANE Select	ENSP00000221138.4:n.*122G>T
ENST00000221138.8:c.*122G>T	ENSP00000221138.4:n.*122G>T
ENST00000518532.1:n.562G>T
ENST00000518564.1:c.142-124G>T	ENSP00000428142.1:n.142-124G>T
ENST00000523023.1:c.181+98G>T
NM_001009552.1:c.*122G>T	NP_001009552.1:n.*122G>T
NM_001009552.2:c.*122G>T MANE Select	NP_001009552.1:n.*122G>T