Canonical Allele Identifier: CA2686824503
Gene: PPP2CB HGNC NCBI

Linked Data

gnomAD v4: 8-30786216-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.30786216C>T , CM000670.2:g.30786216C>T GRCh38
NC_000008.10:g.30643732C>T , CM000670.1:g.30643732C>T GRCh37
NC_000008.9:g.30763274C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000221138.9:c.*19G>A MANE Select ENSP00000221138.4:n.*19G>A
ENST00000221138.8:c.*19G>A ENSP00000221138.4:n.*19G>A
ENST00000518532.1:n.459G>A
ENST00000518564.1:c.142-227G>A ENSP00000428142.1:n.142-227G>A
ENST00000522113.1:n.149G>A
ENST00000523023.1:c.176G>A
NM_001009552.1:c.*19G>A NP_001009552.1:n.*19G>A
NM_001009552.2:c.*19G>A MANE Select NP_001009552.1:n.*19G>A
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