Canonical Allele Identifier: CA607557473
Gene: PPP1CC HGNC NCBI

Linked Data

dbSNP Id: rs1173013701
gnomAD v2: 12-111155043-G-A
gnomAD v3: 12-110717238-G-A
gnomAD v4: 12-110717238-G-A
MyVariant Identifiers: chr12:g.111155043G>A (hg19) chr12:g.110717238G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717238G>A , CM000674.2:g.110717238G>A GRCh38
NC_000012.11:g.111155043G>A , CM000674.1:g.111155043G>A GRCh37
NC_000012.10:g.109639426G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538504.1:c.944-2091C>T XP_011536806.1:n.944-2091C>T
XM_011538505.1:c.943+3867C>T XP_011536807.1:n.943+3867C>T
XM_011538504.3:c.944-2091C>T XP_011536806.1:n.944-2091C>T
XM_011538505.3:c.943+3867C>T XP_011536807.1:n.943+3867C>T
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