Canonical Allele Identifier: CA683538204
Gene: PPP1CC HGNC NCBI

Linked Data

dbSNP Id: rs1341517094
gnomAD v3: 12-110717323-T-C
gnomAD v4: 12-110717323-T-C
MyVariant Identifiers: chr12:g.111155128T>C (hg19) chr12:g.110717323T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717323T>C , CM000674.2:g.110717323T>C GRCh38
NC_000012.11:g.111155128T>C , CM000674.1:g.111155128T>C GRCh37
NC_000012.10:g.109639511T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538504.1:c.944-2176A>G XP_011536806.1:n.944-2176A>G
XM_011538505.1:c.943+3782A>G XP_011536807.1:n.943+3782A>G
XM_011538504.3:c.944-2176A>G XP_011536806.1:n.944-2176A>G
XM_011538505.3:c.943+3782A>G XP_011536807.1:n.943+3782A>G
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