Linked Data
dbSNP Id:
rs1063538
gnomAD v2:
3-186574183-T-C
gnomAD v3:
3-186856394-T-C
gnomAD v4:
3-186856394-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.186856394T>C , CM000665.2:g.186856394T>C | GRCh38 |
| NC_000003.11:g.186574183T>C , CM000665.1:g.186574183T>C | GRCh37 |
| NC_000003.10:g.188056877T>C | NCBI36 |
| NG_021140.1:g.18721T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000320741.7:c.*1690T>C (ADIPOQ) MANE Select | ENSP00000320709.2:n.*1690T>C | |
| ENST00000320741.6:c.*1690T>C (ADIPOQ) | ENSP00000320709.2:n.*1690T>C | |
| ENST00000444204.2:c.*1690T>C (ADIPOQ) | ENSP00000389814.2:n.*1690T>C | |
| NM_001177800.1:c.*1690T>C (ADIPOQ) | NP_001171271.1:n.*1690T>C | |
| NM_004797.3:c.*1690T>C (ADIPOQ) | NP_004788.1:n.*1690T>C | |
| XM_011513324.1:c.*1690T>C (ADIPOQ) | XP_011511626.1:n.*1690T>C | |
| NR_046662.2:n.137-278A>G (ADIPOQ-AS1) | ||
| NM_004797.4:c.*1690T>C (ADIPOQ) MANE Select | NP_004788.1:n.*1690T>C | |
| NM_001177800.2:c.*1690T>C (ADIPOQ) | NP_001171271.1:n.*1690T>C |