Canonical Allele Identifier: CA2686824485
Gene: PPP2CB HGNC NCBI

Linked Data

gnomAD v4: 8-30786194-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.30786194G>T , CM000670.2:g.30786194G>T GRCh38
NC_000008.10:g.30643710G>T , CM000670.1:g.30643710G>T GRCh37
NC_000008.9:g.30763252G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000221138.9:c.*41C>A MANE Select ENSP00000221138.4:n.*41C>A
ENST00000221138.8:c.*41C>A ENSP00000221138.4:n.*41C>A
ENST00000518532.1:n.481C>A
ENST00000518564.1:c.142-205C>A ENSP00000428142.1:n.142-205C>A
ENST00000522113.1:n.171C>A
ENST00000523023.1:c.181+17C>A
NM_001009552.1:c.*41C>A NP_001009552.1:n.*41C>A
NM_001009552.2:c.*41C>A MANE Select NP_001009552.1:n.*41C>A
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