Linked Data
gnomAD v4:
15-74755349-TCA-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74755350_74755351del , CM000677.2:g.74755350_74755351del | GRCh38 |
| NC_000015.9:g.75047691_75047692del , CM000677.1:g.75047691_75047692del | GRCh37 |
| NC_000015.8:g.72834744_72834745del | NCBI36 |
| NG_008431.1:g.37809_37810del | |
| NG_008431.2:g.37809_37810del | |
| NG_061543.1:g.11506_11507del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.*262_*263del MANE Select | ENSP00000342007.4:n.*262_*263del | |
| ENST00000343932.4:c.*262_*263del | ENSP00000342007.4:n.*262_*263del | |
| NM_000761.4:c.*262_*263del | NP_000752.2:n.*262_*263del | |
| NM_000761.5:c.*262_*263del MANE Select | NP_000752.2:n.*262_*263del |