Canonical Allele Identifier: CA2062961031
Gene: PPP1CC HGNC NCBI

Linked Data

dbSNP Id: rs2069699467
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717814G>A , CM000674.2:g.110717814G>A GRCh38
NC_000012.11:g.111155619G>A , CM000674.1:g.111155619G>A GRCh37
NC_000012.10:g.109640002G>A NCBI36
NG_030325.1:g.30165C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011538504.1:c.944-2667C>T XP_011536806.1:n.944-2667C>T
XM_011538505.1:c.943+3291C>T XP_011536807.1:n.943+3291C>T
XM_011538504.3:c.944-2667C>T XP_011536806.1:n.944-2667C>T
XM_011538505.3:c.943+3291C>T XP_011536807.1:n.943+3291C>T
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