Canonical Allele Identifier: CA607557527

Gene: PPP1CC

Linked Data

• dbSNP Id: rs1214299087
• gnomAD v2: 12-111155625-TG-T
• gnomAD v3: 12-110717820-TG-T
• gnomAD v4: 12-110717820-TG-T
• MyVariant Identifiers: chr12:g.111155626del (hg19) ; chr12:g.110717821del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110717822del , CM000674.2:g.110717822del	GRCh38
NC_000012.11:g.111155627del , CM000674.1:g.111155627del	GRCh37
NC_000012.10:g.109640010del	NCBI36
NG_030325.1:g.30158del

Transcript Alleles

HGVS	Amino-acid Change
XM_011538504.1:c.944-2674del	XP_011536806.1:n.944-2674del
XM_011538505.1:c.943+3284del	XP_011536807.1:n.943+3284del
XM_011538504.3:c.944-2674del	XP_011536806.1:n.944-2674del
XM_011538505.3:c.943+3284del	XP_011536807.1:n.943+3284del