Canonical Allele Identifier: CA1346152190
Gene: PPARG HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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