Canonical Allele Identifier: CA951799489
Gene: PPP1CC HGNC NCBI

Linked Data

dbSNP Id: rs2069699732

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717836T>C , CM000674.2:g.110717836T>C GRCh38
NC_000012.11:g.111155641T>C , CM000674.1:g.111155641T>C GRCh37
NC_000012.10:g.109640024T>C NCBI36
NG_030325.1:g.30143A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011538504.1:c.944-2689A>G XP_011536806.1:n.944-2689A>G
XM_011538505.1:c.943+3269A>G XP_011536807.1:n.943+3269A>G
XM_011538504.3:c.944-2689A>G XP_011536806.1:n.944-2689A>G
XM_011538505.3:c.943+3269A>G XP_011536807.1:n.943+3269A>G