Linked Data
gnomAD v4:
10-93601738-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.93601738A>G , CM000672.2:g.93601738A>G | GRCh38 |
| NC_000010.10:g.95361495A>G , CM000672.1:g.95361495A>G | GRCh37 |
| NC_000010.9:g.95351485A>G | NCBI36 |
| NG_009104.1:g.4499T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371469.2:c.-22T>C (RBP4) | ENSP00000360524.2:n.-22T>C | |
| ENST00000604414.1:c.697-2336A>G (FFAR4) | ENSP00000474477.1:n.697-2336A>G | |
| NM_001323518.1:c.-22T>C (RBP4) | NP_001310447.1:n.-22T>C | |
| NM_001323518.2:c.-22T>C (RBP4) | NP_001310447.1:n.-22T>C |