Linked Data
gnomAD v4:
22-20887904-AT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.20887907del , CM000684.2:g.20887907del | GRCh38 |
| NC_000022.10:g.21242195del , CM000684.1:g.21242195del | GRCh37 |
| NC_000022.9:g.19572195del | NCBI36 |
| NG_012152.1:g.33904del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000215730.12:c.*71del MANE Select | ENSP00000215730.6:n.*71del | |
| ENST00000215730.11:c.*71del | ENSP00000215730.6:n.*71del | |
| NM_004782.3:c.*71del | NP_004773.1:n.*71del | |
| NM_004782.4:c.*71del MANE Select | NP_004773.1:n.*71del |