Linked Data
gnomAD v4:
10-122506550-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122506550A>T , CM000672.2:g.122506550A>T | GRCh38 |
| NC_000010.10:g.124266066A>T , CM000672.1:g.124266066A>T | GRCh37 |
| NC_000010.9:g.124256056A>T | NCBI36 |
| NG_011554.1:g.50026A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.778-141A>T MANE Select | ENSP00000357980.3:n.778-141A>T | |
| ENST00000648167.1:c.460-141A>T | ENSP00000498033.1:n.460-141A>T | |
| ENST00000368984.7:c.778-141A>T | ENSP00000357980.3:n.778-141A>T | |
| NM_002775.4:c.778-141A>T | NP_002766.1:n.778-141A>T | |
| NM_002775.5:c.778-141A>T MANE Select | NP_002766.1:n.778-141A>T |