Canonical Allele Identifier: CA243945437
Gene: PPP1CC HGNC NCBI

Linked Data

dbSNP Id: rs774374210
gnomAD v3: 12-110717803-TA-T
gnomAD v4: 12-110717803-TA-T
MyVariant Identifiers: chr12:g.111155609del (hg19) chr12:g.110717804del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717805del , CM000674.2:g.110717805del GRCh38
NC_000012.11:g.111155610del , CM000674.1:g.111155610del GRCh37
NC_000012.10:g.109639993del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538504.1:c.944-2657del XP_011536806.1:n.944-2657del
XM_011538505.1:c.943+3301del XP_011536807.1:n.943+3301del
XM_011538504.3:c.944-2657del XP_011536806.1:n.944-2657del
XM_011538505.3:c.943+3301del XP_011536807.1:n.943+3301del
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