Linked Data
gnomAD v4:
10-122461634-CG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122461635del , CM000672.2:g.122461635del | GRCh38 |
| NC_000010.10:g.124221151del , CM000672.1:g.124221151del | GRCh37 |
| NC_000010.9:g.124211141del | NCBI36 |
| NG_011554.1:g.5111del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.-18del MANE Select | ENSP00000357980.3:n.-18del | |
| ENST00000648167.1:c.154+2926del | ENSP00000498033.1:n.154+2926del | |
| ENST00000368984.7:c.-18del | ENSP00000357980.3:n.-18del | |
| NM_002775.4:c.-18del | NP_002766.1:n.-18del | |
| NM_002775.5:c.-18del MANE Select | NP_002766.1:n.-18del |