Linked Data
gnomAD v4:
10-93601742-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.93601742G>A , CM000672.2:g.93601742G>A | GRCh38 |
| NC_000010.10:g.95361499G>A , CM000672.1:g.95361499G>A | GRCh37 |
| NC_000010.9:g.95351489G>A | NCBI36 |
| NG_009104.1:g.4495C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371469.2:c.-26C>T (RBP4) | ENSP00000360524.2:n.-26C>T | |
| ENST00000604414.1:c.697-2332G>A (FFAR4) | ENSP00000474477.1:n.697-2332G>A | |
| NM_001323518.1:c.-26C>T (RBP4) | NP_001310447.1:n.-26C>T | |
| NM_001323518.2:c.-26C>T (RBP4) | NP_001310447.1:n.-26C>T |