Canonical Allele Identifier: CA2062960649
Gene: PPP1CC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717536T= , CM000674.2:g.110717536T= GRCh38
NC_000012.11:g.111155341T= , CM000674.1:g.111155341T= GRCh37
NC_000012.10:g.109639724T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538504.1:c.944-2389A= XP_011536806.1:n.944-2389A=
XM_011538505.1:c.943+3569A= XP_011536807.1:n.943+3569A=
XM_011538504.3:c.944-2389A= XP_011536806.1:n.944-2389A=
XM_011538505.3:c.943+3569A= XP_011536807.1:n.943+3569A=