Canonical Allele Identifier: CA683538244
Gene: PPP1CC HGNC NCBI

Linked Data

dbSNP Id: rs1261886729
gnomAD v3: 12-110717415-TAA-T
gnomAD v4: 12-110717415-TAA-T
MyVariant Identifiers: chr12:g.111155221_111155222del (hg19) chr12:g.110717416_110717417del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717416_110717417del , CM000674.2:g.110717416_110717417del GRCh38
NC_000012.11:g.111155221_111155222del , CM000674.1:g.111155221_111155222del GRCh37
NC_000012.10:g.109639604_109639605del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538504.1:c.944-2270_944-2269del XP_011536806.1:n.944-2270_944-2269del
XM_011538505.1:c.943+3688_943+3689del XP_011536807.1:n.943+3688_943+3689del
XM_011538504.3:c.944-2270_944-2269del XP_011536806.1:n.944-2270_944-2269del
XM_011538505.3:c.943+3688_943+3689del XP_011536807.1:n.943+3688_943+3689del
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