Canonical Allele Identifier: CA850683875
Gene: PPP2CB HGNC NCBI

Linked Data

dbSNP Id: rs1463828150
gnomAD v3: 8-30786219-G-T
gnomAD v4: 8-30786219-G-T
MyVariant Identifiers: chr8:g.30643735G>T (hg19) chr8:g.30786219G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.30786219G>T , CM000670.2:g.30786219G>T GRCh38
NC_000008.10:g.30643735G>T , CM000670.1:g.30643735G>T GRCh37
NC_000008.9:g.30763277G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000221138.9:c.*16C>A MANE Select ENSP00000221138.4:n.*16C>A
ENST00000221138.8:c.*16C>A ENSP00000221138.4:n.*16C>A
ENST00000518532.1:n.456C>A
ENST00000518564.1:c.142-230C>A ENSP00000428142.1:n.142-230C>A
ENST00000522113.1:n.146C>A
ENST00000523023.1:c.173C>A
NM_001009552.1:c.*16C>A NP_001009552.1:n.*16C>A
NM_001009552.2:c.*16C>A MANE Select NP_001009552.1:n.*16C>A
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