Canonical Allele Identifier: CA607557502
Gene: PPP1CC HGNC NCBI

Linked Data

dbSNP Id: rs1369725821
gnomAD v2: 12-111155340-A-G
gnomAD v3: 12-110717535-A-G
gnomAD v4: 12-110717535-A-G
MyVariant Identifiers: chr12:g.111155340A>G (hg19) chr12:g.110717535A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717535A>G , CM000674.2:g.110717535A>G GRCh38
NC_000012.11:g.111155340A>G , CM000674.1:g.111155340A>G GRCh37
NC_000012.10:g.109639723A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538504.1:c.944-2388T>C XP_011536806.1:n.944-2388T>C
XM_011538505.1:c.943+3570T>C XP_011536807.1:n.943+3570T>C
XM_011538504.3:c.944-2388T>C XP_011536806.1:n.944-2388T>C
XM_011538505.3:c.943+3570T>C XP_011536807.1:n.943+3570T>C
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