Canonical Allele Identifier: CA683538402
Gene: PPP1CC HGNC NCBI

Linked Data

dbSNP Id: rs1283696056
gnomAD v3: 12-110717685-C-T
gnomAD v4: 12-110717685-C-T
MyVariant Identifiers: chr12:g.111155490C>T (hg19) chr12:g.110717685C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717685C>T , CM000674.2:g.110717685C>T GRCh38
NC_000012.11:g.111155490C>T , CM000674.1:g.111155490C>T GRCh37
NC_000012.10:g.109639873C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011538504.1:c.944-2538G>A XP_011536806.1:n.944-2538G>A
XM_011538505.1:c.943+3420G>A XP_011536807.1:n.943+3420G>A
XM_011538504.3:c.944-2538G>A XP_011536806.1:n.944-2538G>A
XM_011538505.3:c.943+3420G>A XP_011536807.1:n.943+3420G>A
Search 100 bp 5'
Search 100 bp 3'