Canonical Allele Identifier: CA11436966
Gene: PPARG HGNC NCBI
MyVariant.info:
GRCh38 chr3:g.12287696G>C
GRCh37 chr3:g.12329195G>C
gnomAD v2:
3:12329195 G / C
gnomAD v3:
3:12287696 G / C
gnomAD v4:
chr3-12287696-G-C
Joint Max Group AF 0.7332181 (EAS)
Genomes Max Group AF 0.73340141 (EAS)
Exomes Max Group AF 0.26597318 (NFE)
dbSNP:
2920502
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12287696G>C , CM000665.2:g.12287696G>C GRCh38
NC_000003.11:g.12329195G>C , CM000665.1:g.12329195G>C GRCh37
NC_000003.10:g.12304195G>C NCBI36
NG_011749.1:g.4847G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000397010.7:c.-83+21G>C ENSP00000380205.3:n.-83+21G>C
ENST00000397029.8:c.-9+21G>C ENSP00000380224.4:n.-9+21G>C
ENST00000397010.6:c.-77+21G>C ENSP00000380205.2:n.-77+21G>C
ENST00000397029.7:c.-3+21G>C ENSP00000380224.3:n.-3+21G>C
NM_001354666.1:c.-77+21G>C NP_001341595.1:n.-77+21G>C
NM_001354666.2:c.-77+21G>C NP_001341595.1:n.-77+21G>C
NM_001354666.3:c.-83+21G>C NP_001341595.2:n.-83+21G>C
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