Canonical Allele Identifier: CA683538222
Gene: PPP1CC HGNC NCBI

Linked Data

dbSNP Id: rs1173778319
MyVariant Identifiers: chr12:g.111155145_111155146del (hg19) chr12:g.110717340_110717341del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717340_110717341del , CM000674.2:g.110717340_110717341del GRCh38
NC_000012.11:g.111155145_111155146del , CM000674.1:g.111155145_111155146del GRCh37
NC_000012.10:g.109639528_109639529del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538504.1:c.944-2194_944-2193del XP_011536806.1:n.944-2194_944-2193del
XM_011538505.1:c.943+3764_943+3765del XP_011536807.1:n.943+3764_943+3765del
XM_011538504.3:c.944-2194_944-2193del XP_011536806.1:n.944-2194_944-2193del
XM_011538505.3:c.943+3764_943+3765del XP_011536807.1:n.943+3764_943+3765del
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