Canonical Allele Identifier: CA174837005
Gene: PPP2CB HGNC NCBI

Linked Data

dbSNP Id: rs369673074
MyVariant Identifiers: chr8:g.30643624A>C (hg19) chr8:g.30786108A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.30786108A>C , CM000670.2:g.30786108A>C GRCh38
NC_000008.10:g.30643624A>C , CM000670.1:g.30643624A>C GRCh37
NC_000008.9:g.30763166A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000221138.9:c.*127T>G MANE Select ENSP00000221138.4:n.*127T>G
ENST00000221138.8:c.*127T>G ENSP00000221138.4:n.*127T>G
ENST00000518564.1:c.142-119T>G ENSP00000428142.1:n.142-119T>G
ENST00000523023.1:c.181+103T>G
NM_001009552.1:c.*127T>G NP_001009552.1:n.*127T>G
NM_001009552.2:c.*127T>G MANE Select NP_001009552.1:n.*127T>G
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