Revel Score:
ENST00000330597 (MANE Select)
0.487
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5248400C>T , CM000673.2:g.5248400C>T | GRCh38 |
| NC_000011.9:g.5269630C>T , CM000673.1:g.5269630C>T | GRCh37 |
| NC_000011.8:g.5226206C>T | NCBI36 |
| NG_000007.3:g.49216G>A | |
| NG_063112.2:g.258G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330597.5:c.403G>A (HBG1) MANE Select | ENSP00000327431.4:p.Val135Met | |
| ENST00000642908.1:c.403G>A | ENSP00000495346.1:p.Val135Met | |
| ENST00000647543.1:c.466G>A | ENSP00000496470.1:p.Val156Met | |
| ENST00000648735.1:n.1334G>A (HBG1) | ||
| ENST00000330597.3:c.403G>A (HBG1) | ENSP00000327431.3:p.Val135Met | |
| ENST00000620888.4:c.403G>A (HBG2) | ENSP00000479637.1:p.Val135Met | |
| NM_000559.2:c.403G>A (HBG1) | NP_000550.2:p.Val135Met | |
| NM_000559.3:c.403G>A (HBG1) MANE Select | NP_000550.2:p.Val135Met |