Canonical Allele Identifier: CA2686824448
Gene: PPP2CB HGNC NCBI

Linked Data

dbSNP Id: rs1806336399
gnomAD v4: 8-30786125-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.30786125C>A , CM000670.2:g.30786125C>A GRCh38
NC_000008.10:g.30643641C>A , CM000670.1:g.30643641C>A GRCh37
NC_000008.9:g.30763183C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000221138.9:c.*110G>T MANE Select ENSP00000221138.4:n.*110G>T
ENST00000221138.8:c.*110G>T ENSP00000221138.4:n.*110G>T
ENST00000518532.1:n.550G>T
ENST00000518564.1:c.142-136G>T ENSP00000428142.1:n.142-136G>T
ENST00000523023.1:c.181+86G>T
NM_001009552.1:c.*110G>T NP_001009552.1:n.*110G>T
NM_001009552.2:c.*110G>T MANE Select NP_001009552.1:n.*110G>T
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