Canonical Allele Identifier: CA2686824501
Gene: PPP2CB HGNC NCBI

Linked Data

gnomAD v4: 8-30786215-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.30786215G>T , CM000670.2:g.30786215G>T GRCh38
NC_000008.10:g.30643731G>T , CM000670.1:g.30643731G>T GRCh37
NC_000008.9:g.30763273G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000221138.9:c.*20C>A MANE Select ENSP00000221138.4:n.*20C>A
ENST00000221138.8:c.*20C>A ENSP00000221138.4:n.*20C>A
ENST00000518532.1:n.460C>A
ENST00000518564.1:c.142-226C>A ENSP00000428142.1:n.142-226C>A
ENST00000522113.1:n.150C>A
ENST00000523023.1:c.177C>A
NM_001009552.1:c.*20C>A NP_001009552.1:n.*20C>A
NM_001009552.2:c.*20C>A MANE Select NP_001009552.1:n.*20C>A
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