Canonical Allele Identifier: CA2686824446
Gene: PPP2CB HGNC NCBI

Linked Data

gnomAD v4: 8-30786122-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.30786122T>A , CM000670.2:g.30786122T>A GRCh38
NC_000008.10:g.30643638T>A , CM000670.1:g.30643638T>A GRCh37
NC_000008.9:g.30763180T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000221138.9:c.*113A>T MANE Select ENSP00000221138.4:n.*113A>T
ENST00000221138.8:c.*113A>T ENSP00000221138.4:n.*113A>T
ENST00000518532.1:n.553A>T
ENST00000518564.1:c.142-133A>T ENSP00000428142.1:n.142-133A>T
ENST00000523023.1:c.181+89A>T
NM_001009552.1:c.*113A>T NP_001009552.1:n.*113A>T
NM_001009552.2:c.*113A>T MANE Select NP_001009552.1:n.*113A>T