Linked Data
gnomAD v4:
10-122461612-TCG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122461614_122461615del , CM000672.2:g.122461614_122461615del | GRCh38 |
| NC_000010.10:g.124221130_124221131del , CM000672.1:g.124221130_124221131del | GRCh37 |
| NC_000010.9:g.124211120_124211121del | NCBI36 |
| NG_011554.1:g.5090_5091del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.-39_-38del MANE Select | ENSP00000357980.3:n.-39_-38del | |
| ENST00000648167.1:c.154+2905_154+2906del | ENSP00000498033.1:n.154+2905_154+2906del | |
| ENST00000368984.7:c.-39_-38del | ENSP00000357980.3:n.-39_-38del | |
| NM_002775.4:c.-39_-38del | NP_002766.1:n.-39_-38del | |
| NM_002775.5:c.-39_-38del MANE Select | NP_002766.1:n.-39_-38del |