Canonical Allele Identifier: CA13675420

Gene: PPP1CC

Linked Data

• dbSNP Id: rs118122911
• gnomAD v2: 12-111155321-C-G
• gnomAD v3: 12-110717516-C-G
• gnomAD v4: 12-110717516-C-G
• MyVariant Identifiers: chr12:g.111155321C>G (hg19) ; chr12:g.110717516C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110717516C>G , CM000674.2:g.110717516C>G	GRCh38
NC_000012.11:g.111155321C>G , CM000674.1:g.111155321C>G	GRCh37
NC_000012.10:g.109639704C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011538504.1:c.944-2369G>C	XP_011536806.1:n.944-2369G>C
XM_011538505.1:c.943+3589G>C	XP_011536807.1:n.943+3589G>C
XM_011538504.3:c.944-2369G>C	XP_011536806.1:n.944-2369G>C
XM_011538505.3:c.943+3589G>C	XP_011536807.1:n.943+3589G>C