Linked Data
gnomAD v4:
10-122461624-CCG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122461626_122461627del , CM000672.2:g.122461626_122461627del | GRCh38 |
| NC_000010.10:g.124221142_124221143del , CM000672.1:g.124221142_124221143del | GRCh37 |
| NC_000010.9:g.124211132_124211133del | NCBI36 |
| NG_011554.1:g.5102_5103del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.-27_-26del MANE Select | ENSP00000357980.3:n.-27_-26del | |
| ENST00000648167.1:c.154+2917_154+2918del | ENSP00000498033.1:n.154+2917_154+2918del | |
| ENST00000368984.7:c.-27_-26del | ENSP00000357980.3:n.-27_-26del | |
| NM_002775.4:c.-27_-26del | NP_002766.1:n.-27_-26del | |
| NM_002775.5:c.-27_-26del MANE Select | NP_002766.1:n.-27_-26del |