Canonical Allele Identifier: CA2838419344
Gene: PPARG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12446154C>A , CM000665.2:g.12446154C>A GRCh38
NC_000003.11:g.12487653C>A , CM000665.1:g.12487653C>A GRCh37
NC_000003.10:g.12462653C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011533842.1:c.1271-24667C>A XP_011532144.1:n.1271-24667C>A
XM_011533842.2:c.1271-24667C>A XP_011532144.1:n.1271-24667C>A