Canonical Allele Identifier: CA2686824429
Gene: PPP2CB HGNC NCBI

Linked Data

gnomAD v4: 8-30786100-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.30786100T>C , CM000670.2:g.30786100T>C GRCh38
NC_000008.10:g.30643616T>C , CM000670.1:g.30643616T>C GRCh37
NC_000008.9:g.30763158T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000221138.9:c.*135A>G MANE Select ENSP00000221138.4:n.*135A>G
ENST00000221138.8:c.*135A>G ENSP00000221138.4:n.*135A>G
ENST00000518564.1:c.142-111A>G ENSP00000428142.1:n.142-111A>G
ENST00000523023.1:c.181+111A>G
NM_001009552.1:c.*135A>G NP_001009552.1:n.*135A>G
NM_001009552.2:c.*135A>G MANE Select NP_001009552.1:n.*135A>G