Linked Data
gnomAD v4:
20-3082944-C-CA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.3082944_3082945insA , CM000682.2:g.3082944_3082945insA | GRCh38 |
| NC_000020.10:g.3063590_3063591insA , CM000682.1:g.3063590_3063591insA | GRCh37 |
| NC_000020.9:g.3011590_3011591insA | NCBI36 |
| NG_008663.1:g.6780_6781insT , LRG_715:g.6780_6781insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380293.3:c.322+32_322+33insT MANE Select | ENSP00000369647.3:n.322+32_322+33insT | |
| NM_000490.4:c.322+32_322+33insT , LRG_715t1:c.322+32_322+33insT | NP_000481.2:n.322+32_322+33insT | |
| XM_011529267.1:c.322+32_322+33insT | XP_011527569.1:n.322+32_322+33insT | |
| XM_011529267.2:c.322+32_322+33insT | XP_011527569.1:n.322+32_322+33insT | |
| NM_000490.5:c.322+32_322+33insT MANE Select | NP_000481.2:n.322+32_322+33insT |