Canonical Allele Identifier: CA243945439
Gene: PPP1CC HGNC NCBI

Linked Data

dbSNP Id: rs920620402
gnomAD v3: 12-110717832-C-T
gnomAD v4: 12-110717832-C-T
MyVariant Identifiers: chr12:g.111155637C>T (hg19) chr12:g.110717832C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717832C>T , CM000674.2:g.110717832C>T GRCh38
NC_000012.11:g.111155637C>T , CM000674.1:g.111155637C>T GRCh37
NC_000012.10:g.109640020C>T NCBI36
NG_030325.1:g.30147G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011538504.1:c.944-2685G>A XP_011536806.1:n.944-2685G>A
XM_011538505.1:c.943+3273G>A XP_011536807.1:n.943+3273G>A
XM_011538504.3:c.944-2685G>A XP_011536806.1:n.944-2685G>A
XM_011538505.3:c.943+3273G>A XP_011536807.1:n.943+3273G>A
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