gnomAD v2:
gnomAD v3:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.186853334G>C , CM000665.2:g.186853334G>C | GRCh38 |
| NC_000003.11:g.186571123G>C , CM000665.1:g.186571123G>C | GRCh37 |
| NC_000003.10:g.188053817G>C | NCBI36 |
| NG_021140.1:g.15661G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320741.7:c.214+62G>C (ADIPOQ) MANE Select | ENSP00000320709.2:n.214+62G>C | |
| ENST00000320741.6:c.214+62G>C (ADIPOQ) | ENSP00000320709.2:n.214+62G>C | |
| ENST00000444204.2:c.214+62G>C (ADIPOQ) | ENSP00000389814.2:n.214+62G>C | |
| NM_001177800.1:c.214+62G>C (ADIPOQ) | NP_001171271.1:n.214+62G>C | |
| NM_004797.3:c.214+62G>C (ADIPOQ) | NP_004788.1:n.214+62G>C | |
| NR_046662.1:n.2087-92C>G (ADIPOQ-AS1) | ||
| XM_011513324.1:c.214+62G>C (ADIPOQ) | XP_011511626.1:n.214+62G>C | |
| NR_046662.2:n.2216-92C>G (ADIPOQ-AS1) | ||
| NM_004797.4:c.214+62G>C (ADIPOQ) MANE Select | NP_004788.1:n.214+62G>C | |
| NM_001177800.2:c.214+62G>C (ADIPOQ) | NP_001171271.1:n.214+62G>C |