Canonical Allele Identifier: CA683538236

Gene: PPP1CC

Linked Data

• dbSNP Id: rs1020689958
• gnomAD v3: 12-110717404-C-T
• gnomAD v4: 12-110717404-C-T
• MyVariant Identifiers: chr12:g.111155209C>T (hg19) ; chr12:g.110717404C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110717404C>T , CM000674.2:g.110717404C>T	GRCh38
NC_000012.11:g.111155209C>T , CM000674.1:g.111155209C>T	GRCh37
NC_000012.10:g.109639592C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011538504.1:c.944-2257G>A	XP_011536806.1:n.944-2257G>A
XM_011538505.1:c.943+3701G>A	XP_011536807.1:n.943+3701G>A
XM_011538504.3:c.944-2257G>A	XP_011536806.1:n.944-2257G>A
XM_011538505.3:c.943+3701G>A	XP_011536807.1:n.943+3701G>A