Canonical Allele Identifier: CA13632580

Gene: PPP1CC

Linked Data

• dbSNP Id: rs57865940
• gnomAD v2: 12-111155491-A-G
• gnomAD v3: 12-110717686-A-G
• gnomAD v4: 12-110717686-A-G
• MyVariant Identifiers: chr12:g.111155491A>G (hg19) ; chr12:g.110717686A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110717686A>G , CM000674.2:g.110717686A>G	GRCh38
NC_000012.11:g.111155491A>G , CM000674.1:g.111155491A>G	GRCh37
NC_000012.10:g.109639874A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011538504.1:c.944-2539T>C	XP_011536806.1:n.944-2539T>C
XM_011538505.1:c.943+3419T>C	XP_011536807.1:n.943+3419T>C
XM_011538504.3:c.944-2539T>C	XP_011536806.1:n.944-2539T>C
XM_011538505.3:c.943+3419T>C	XP_011536807.1:n.943+3419T>C