Canonical Allele Identifier: CA2686824468
Gene: PPP2CB HGNC NCBI

Linked Data

gnomAD v4: 8-30786157-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.30786157G>T , CM000670.2:g.30786157G>T GRCh38
NC_000008.10:g.30643673G>T , CM000670.1:g.30643673G>T GRCh37
NC_000008.9:g.30763215G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000221138.9:c.*78C>A MANE Select ENSP00000221138.4:n.*78C>A
ENST00000221138.8:c.*78C>A ENSP00000221138.4:n.*78C>A
ENST00000518532.1:n.518C>A
ENST00000518564.1:c.142-168C>A ENSP00000428142.1:n.142-168C>A
ENST00000522113.1:n.208C>A
ENST00000523023.1:c.181+54C>A
NM_001009552.1:c.*78C>A NP_001009552.1:n.*78C>A
NM_001009552.2:c.*78C>A MANE Select NP_001009552.1:n.*78C>A
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