Canonical Allele Identifier: CA243945446
Gene: PPP1CC HGNC NCBI

Linked Data

dbSNP Id: rs1040876525
gnomAD v3: 12-110717866-G-A
gnomAD v4: 12-110717866-G-A
MyVariant Identifiers: chr12:g.111155671G>A (hg19) chr12:g.110717866G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717866G>A , CM000674.2:g.110717866G>A GRCh38
NC_000012.11:g.111155671G>A , CM000674.1:g.111155671G>A GRCh37
NC_000012.10:g.109640054G>A NCBI36
NG_030325.1:g.30113C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011538504.1:c.944-2719C>T XP_011536806.1:n.944-2719C>T
XM_011538505.1:c.943+3239C>T XP_011536807.1:n.943+3239C>T
XM_011538504.3:c.944-2719C>T XP_011536806.1:n.944-2719C>T
XM_011538505.3:c.943+3239C>T XP_011536807.1:n.943+3239C>T
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