Linked Data
gnomAD v4:
20-46011131-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46011132del , CM000682.2:g.46011132del | GRCh38 |
| NC_000020.10:g.44639771del , CM000682.1:g.44639771del | GRCh37 |
| NC_000020.9:g.44073178del | NCBI36 |
| NG_011468.1:g.7225del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372330.3:c.650-11del MANE Select | ENSP00000361405.3:n.650-11del | |
| NM_004994.2:c.650-11del | NP_004985.2:n.650-11del | |
| NM_004994.3:c.650-11del MANE Select | NP_004985.2:n.650-11del |