Linked Data
gnomAD v4:
10-93601634-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.93601634G>T , CM000672.2:g.93601634G>T | GRCh38 |
| NC_000010.10:g.95361391G>T , CM000672.1:g.95361391G>T | GRCh37 |
| NC_000010.9:g.95351381G>T | NCBI36 |
| NG_009104.1:g.4603C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371467.5:c.-291C>A (RBP4) | ENSP00000360522.1:n.-291C>A | |
| ENST00000371469.2:c.51+32C>A (RBP4) | ENSP00000360524.2:n.51+32C>A | |
| ENST00000604414.1:c.697-2440G>T (FFAR4) | ENSP00000474477.1:n.697-2440G>T | |
| ENST00000629763.2:c.47+36C>A (RBP4) | ENSP00000487033.1:n.47+36C>A | |
| NM_001323518.1:c.51+32C>A (RBP4) | NP_001310447.1:n.51+32C>A | |
| NM_001323518.2:c.51+32C>A (RBP4) | NP_001310447.1:n.51+32C>A |