Canonical Allele Identifier: CA481849036
Gene: PPP1CC HGNC NCBI

Linked Data

dbSNP Id: rs2069699073
MyVariant Identifiers: chr12:g.111155561C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717756C>A , CM000674.2:g.110717756C>A GRCh38
NC_000012.11:g.111155561C>A , CM000674.1:g.111155561C>A GRCh37
NC_000012.10:g.109639944C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011538504.1:c.944-2609G>T XP_011536806.1:n.944-2609G>T
XM_011538505.1:c.943+3349G>T XP_011536807.1:n.943+3349G>T
XM_011538504.3:c.944-2609G>T XP_011536806.1:n.944-2609G>T
XM_011538505.3:c.943+3349G>T XP_011536807.1:n.943+3349G>T