Linked Data
gnomAD v4:
18-77268548-TCC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.77268549_77268550del , CM000680.2:g.77268549_77268550del | GRCh38 |
| NC_000018.9:g.74980505_74980506del , CM000680.1:g.74980505_74980506del | GRCh37 |
| NC_000018.8:g.73109493_73109494del | NCBI36 |
| NG_009223.1:g.23498_23499del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000299727.5:c.733-36_733-35del MANE Select | ENSP00000299727.3:n.733-36_733-35del | |
| ENST00000299727.4:c.733-36_733-35del | ENSP00000299727.3:n.733-36_733-35del | |
| NM_001480.3:c.733-36_733-35del | NP_001471.2:n.733-36_733-35del | |
| NM_001480.4:c.733-36_733-35del MANE Select | NP_001471.2:n.733-36_733-35del |