Canonical Allele Identifier: CA243945397
Gene: PPP1CC HGNC NCBI

Linked Data

dbSNP Id: rs10083038
gnomAD v2: 12-111155343-C-T
gnomAD v3: 12-110717538-C-T
gnomAD v4: 12-110717538-C-T
MyVariant Identifiers: chr12:g.111155343C>T (hg19) chr12:g.110717538C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717538C>T , CM000674.2:g.110717538C>T GRCh38
NC_000012.11:g.111155343C>T , CM000674.1:g.111155343C>T GRCh37
NC_000012.10:g.109639726C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538504.1:c.944-2391G>A XP_011536806.1:n.944-2391G>A
XM_011538505.1:c.943+3567G>A XP_011536807.1:n.943+3567G>A
XM_011538504.3:c.944-2391G>A XP_011536806.1:n.944-2391G>A
XM_011538505.3:c.943+3567G>A XP_011536807.1:n.943+3567G>A
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