Canonical Allele Identifier: CA1346079995
Gene: PPARG HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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