Linked Data
dbSNP Id:
rs11187545
gnomAD v2:
10-95357105-A-G
gnomAD v3:
10-93597348-A-G
gnomAD v4:
10-93597348-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.93597348A>G , CM000672.2:g.93597348A>G | GRCh38 |
| NC_000010.10:g.95357105A>G , CM000672.1:g.95357105A>G | GRCh37 |
| NC_000010.9:g.95347095A>G | NCBI36 |
| NG_009104.1:g.8889T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371464.8:c.355+3045T>C (RBP4) MANE Select | ENSP00000360519.3:n.355+3045T>C | |
| ENST00000371464.7:c.355+3045T>C (RBP4) | ENSP00000360519.3:n.355+3045T>C | |
| ENST00000371467.5:c.355+3045T>C (RBP4) | ENSP00000360522.1:n.355+3045T>C | |
| ENST00000371469.2:c.349+3045T>C (RBP4) | ENSP00000360524.2:n.349+3045T>C | |
| ENST00000604414.1:c.697-6726A>G (FFAR4) | ENSP00000474477.1:n.697-6726A>G | |
| ENST00000615669.4:c.349+3045T>C (RBP4) | ENSP00000480654.1:n.349+3045T>C | |
| ENST00000629763.2:c.349+3045T>C (RBP4) | ENSP00000487033.1:n.349+3045T>C | |
| NM_006744.3:c.355+3045T>C (RBP4) | NP_006735.2:n.355+3045T>C | |
| NM_001323517.1:c.355+3045T>C (RBP4) | NP_001310446.1:n.355+3045T>C | |
| NM_001323518.1:c.349+3045T>C (RBP4) | NP_001310447.1:n.349+3045T>C | |
| NM_006744.4:c.355+3045T>C (RBP4) MANE Select | NP_006735.2:n.355+3045T>C | |
| NM_001323518.2:c.349+3045T>C (RBP4) | NP_001310447.1:n.349+3045T>C |