Canonical Allele Identifier: CA607557472

Gene: PPP1CC

Linked Data

• dbSNP Id: rs1433420632
• gnomAD v2: 12-111155032-T-TG
• MyVariant Identifiers: chr12:g.111155032_111155033insG (hg19) ; chr12:g.110717227_110717228insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110717231dup , CM000674.2:g.110717231dup	GRCh38
NC_000012.11:g.111155036dup , CM000674.1:g.111155036dup	GRCh37
NC_000012.10:g.109639419dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011538504.1:c.944-2081dup	XP_011536806.1:n.944-2081dup
XM_011538505.1:c.943+3877dup	XP_011536807.1:n.943+3877dup
XM_011538504.3:c.944-2081dup	XP_011536806.1:n.944-2081dup
XM_011538505.3:c.943+3877dup	XP_011536807.1:n.943+3877dup