Canonical Allele Identifier: CA1346152191
Gene: PPARG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12447383G= , CM000665.2:g.12447383G= GRCh38
NC_000003.11:g.12488882G= , CM000665.1:g.12488882G= GRCh37
NC_000003.10:g.12463882G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011533842.1:c.1271-23438G= XP_011532144.1:n.1271-23438G=
XM_011533842.2:c.1271-23438G= XP_011532144.1:n.1271-23438G=