Canonical Allele Identifier: CA15248306
Gene: PPARG HGNC NCBI

Linked Data

dbSNP Id: rs17036314

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12335246G>C , CM000665.2:g.12335246G>C GRCh38
NC_000003.11:g.12376745G>C , CM000665.1:g.12376745G>C GRCh37
NC_000003.10:g.12351745G>C NCBI36
NG_011749.1:g.52397G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000309576.11:c.-9+22793G>C ENSP00000312472.7:p.=
ENST00000397000.6:c.-9+22793G>C ENSP00000380196.2:p.=
ENST00000397010.7:c.-9+22793G>C ENSP00000380205.3:p.=
ENST00000397015.7:c.-8-44458G>C ENSP00000380210.3:p.=
ENST00000397026.7:c.-270+22793G>C ENSP00000380221.3:p.=
ENST00000397029.8:c.-8-44458G>C ENSP00000380224.4:p.=
ENST00000438682.6:c.-9+22793G>C ENSP00000392285.2:p.=
ENST00000455517.6:c.-8-44458G>C ENSP00000411931.2:p.=
ENST00000643197.2:c.-9+22793G>C ENSP00000495840.2:p.=
ENST00000643888.2:c.-96-9561G>C ENSP00000494934.2:p.=
ENST00000644622.2:c.-9+22793G>C ENSP00000494873.2:p.=
ENST00000651735.1:c.-9+22793G>C MANE Select ENSP00000498313.1:p.=
ENST00000652098.1:c.-18+22793G>C ENSP00000498300.1:p.=
ENST00000652431.1:c.-93+22793G>C ENSP00000498717.1:p.=
ENST00000652522.1:c.-9+22793G>C ENSP00000498500.1:p.=
ENST00000309576.10:c.-3+22793G>C ENSP00000312472.6:p.=
ENST00000397000.5:c.-3+22793G>C ENSP00000380196.1:p.=
ENST00000397010.6:c.-3+22793G>C ENSP00000380205.2:p.=
ENST00000397012.6:c.-3+22793G>C ENSP00000380207.2:p.=
ENST00000397015.6:c.-2-44458G>C ENSP00000380210.2:p.=
ENST00000397026.6:c.-246+22793G>C ENSP00000380221.2:p.=
ENST00000397029.7:c.-2-44458G>C ENSP00000380224.3:p.=
ENST00000438682.5:c.-3+22793G>C ENSP00000392285.1:p.=
ENST00000455517.5:c.-2-44458G>C ENSP00000411931.1:p.=
ENST00000497594.5:n.98+22793G>C
NM_005037.5:c.-2-44458G>C NP_005028.4:p.=
NM_138711.3:c.-3+22793G>C NP_619725.2:p.=
NM_138712.3:c.-3+22793G>C NP_619726.2:p.=
XM_011533840.1:c.-3+22793G>C XP_011532142.1:p.=
XM_011533841.1:c.-2-44458G>C XP_011532143.1:p.=
XM_011533844.1:c.-3+22793G>C XP_011532146.1:p.=
NM_001330615.1:c.-3+22793G>C NP_001317544.1:p.=
NM_001354666.1:c.-3+22793G>C NP_001341595.1:p.=
NM_001354667.1:c.-2-44458G>C NP_001341596.1:p.=
NM_001354669.1:c.-436+22793G>C NP_001341598.1:p.=
NM_001354670.1:c.-3+22793G>C NP_001341599.1:p.=
XM_024453604.1:c.-3+22793G>C XP_024309372.1:p.=
XM_024453605.1:c.-3+22793G>C XP_024309373.1:p.=
XM_024453606.1:c.-3+22793G>C XP_024309374.1:p.=
NM_001330615.2:c.-3+22793G>C NP_001317544.1:p.=
NM_001354666.2:c.-3+22793G>C NP_001341595.1:p.=
NM_001354667.2:c.-2-44458G>C NP_001341596.1:p.=
NM_001354669.2:c.-436+22793G>C NP_001341598.1:p.=
NM_001354670.2:c.-3+22793G>C NP_001341599.1:p.=
NM_001374261.1:c.-3+22793G>C NP_001361190.1:p.=
NM_001374262.1:c.-90-9561G>C NP_001361191.1:p.=
NM_001374263.1:c.-3+22793G>C NP_001361192.1:p.=
NM_001374264.1:c.-3+22793G>C NP_001361193.1:p.=
NM_001374266.1:c.-3+22793G>C NP_001361195.1:p.=
NM_005037.6:c.-2-44458G>C NP_005028.4:p.=
NM_138711.4:c.-3+22793G>C NP_619725.2:p.=
NM_138712.4:c.-3+22793G>C NP_619726.2:p.=
NM_001330615.4:c.-9+22793G>C NP_001317544.2:p.=
NM_001354666.3:c.-9+22793G>C NP_001341595.2:p.=
NM_001354667.3:c.-8-44458G>C NP_001341596.2:p.=
NM_001374261.3:c.-9+22793G>C NP_001361190.2:p.=
NM_001374262.3:c.-96-9561G>C NP_001361191.2:p.=
NM_001374263.2:c.-9+22793G>C NP_001361192.2:p.=
NM_001374264.2:c.-9+22793G>C NP_001361193.2:p.=
NM_005037.7:c.-8-44458G>C NP_005028.5:p.=
NM_138711.6:c.-9+22793G>C MANE Select NP_619725.3:p.=
NM_138712.5:c.-9+22793G>C NP_619726.3:p.=