gnomAD v3:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.186857603G>A , CM000665.2:g.186857603G>A | GRCh38 |
| NC_000003.11:g.186575392G>A , CM000665.1:g.186575392G>A | GRCh37 |
| NC_000003.10:g.188058086G>A | NCBI36 |
| NG_021140.1:g.19930G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320741.7:c.*2899G>A (ADIPOQ) MANE Select | ENSP00000320709.2:n.*2899G>A | |
| ENST00000320741.6:c.*2899G>A (ADIPOQ) | ENSP00000320709.2:n.*2899G>A | |
| ENST00000444204.2:c.*2899G>A (ADIPOQ) | ENSP00000389814.2:n.*2899G>A | |
| NM_001177800.1:c.*2899G>A (ADIPOQ) | NP_001171271.1:n.*2899G>A | |
| NM_004797.3:c.*2899G>A (ADIPOQ) | NP_004788.1:n.*2899G>A | |
| XM_011513324.1:c.*2899G>A (ADIPOQ) | XP_011511626.1:n.*2899G>A | |
| NR_046662.2:n.137-1487C>T (ADIPOQ-AS1) | ||
| NM_004797.4:c.*2899G>A (ADIPOQ) MANE Select | NP_004788.1:n.*2899G>A | |
| NM_001177800.2:c.*2899G>A (ADIPOQ) | NP_001171271.1:n.*2899G>A |