Canonical Allele Identifier: CA607557519

Gene: PPP1CC

Linked Data

• dbSNP Id: rs1326400688
• gnomAD v2: 12-111155493-G-A
• gnomAD v3: 12-110717688-G-A
• gnomAD v4: 12-110717688-G-A
• MyVariant Identifiers: chr12:g.111155493G>A (hg19) ; chr12:g.110717688G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110717688G>A , CM000674.2:g.110717688G>A	GRCh38
NC_000012.11:g.111155493G>A , CM000674.1:g.111155493G>A	GRCh37
NC_000012.10:g.109639876G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011538504.1:c.944-2541C>T	XP_011536806.1:n.944-2541C>T
XM_011538505.1:c.943+3417C>T	XP_011536807.1:n.943+3417C>T
XM_011538504.3:c.944-2541C>T	XP_011536806.1:n.944-2541C>T
XM_011538505.3:c.943+3417C>T	XP_011536807.1:n.943+3417C>T