Canonical Allele Identifier: CA951799468
Gene: PPP1CC HGNC NCBI

Linked Data

dbSNP Id: rs2069698927

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717734A>G , CM000674.2:g.110717734A>G GRCh38
NC_000012.11:g.111155539A>G , CM000674.1:g.111155539A>G GRCh37
NC_000012.10:g.109639922A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011538504.1:c.944-2587T>C XP_011536806.1:n.944-2587T>C
XM_011538505.1:c.943+3371T>C XP_011536807.1:n.943+3371T>C
XM_011538504.3:c.944-2587T>C XP_011536806.1:n.944-2587T>C
XM_011538505.3:c.943+3371T>C XP_011536807.1:n.943+3371T>C