Linked Data
gnomAD v4:
20-46011774-AG-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46011775del , CM000682.2:g.46011775del | GRCh38 |
| NC_000020.10:g.44640414del , CM000682.1:g.44640414del | GRCh37 |
| NC_000020.9:g.44073821del | NCBI36 |
| NG_011468.1:g.7868del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372330.3:c.997+28del MANE Select | ENSP00000361405.3:n.997+28del | |
| NM_004994.2:c.997+28del | NP_004985.2:n.997+28del | |
| NM_004994.3:c.997+28del MANE Select | NP_004985.2:n.997+28del |