Canonical Allele Identifier: CA13696111
Gene: PPP1CC HGNC NCBI

Linked Data

dbSNP Id: rs11065706

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717726T>C , CM000674.2:g.110717726T>C GRCh38
NC_000012.11:g.111155531T>C , CM000674.1:g.111155531T>C GRCh37
NC_000012.10:g.109639914T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011538504.1:c.944-2579A>G XP_011536806.1:n.944-2579A>G
XM_011538505.1:c.943+3379A>G XP_011536807.1:n.943+3379A>G
XM_011538504.3:c.944-2579A>G XP_011536806.1:n.944-2579A>G
XM_011538505.3:c.943+3379A>G XP_011536807.1:n.943+3379A>G