Canonical Allele Identifier: CA2062960849
Gene: PPP1CC HGNC NCBI

Linked Data

dbSNP Id: rs2069698371

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717664G>C , CM000674.2:g.110717664G>C GRCh38
NC_000012.11:g.111155469G>C , CM000674.1:g.111155469G>C GRCh37
NC_000012.10:g.109639852G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011538504.1:c.944-2517C>G XP_011536806.1:n.944-2517C>G
XM_011538505.1:c.943+3441C>G XP_011536807.1:n.943+3441C>G
XM_011538504.3:c.944-2517C>G XP_011536806.1:n.944-2517C>G
XM_011538505.3:c.943+3441C>G XP_011536807.1:n.943+3441C>G