Linked Data
gnomAD v4:
9-91950000-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.91950001del , CM000671.2:g.91950001del | GRCh38 |
| NC_000009.11:g.94712283del , CM000671.1:g.94712283del | GRCh37 |
| NC_000009.10:g.93752104del | NCBI36 |
| NG_008089.1:g.5162del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375708.4:c.-38del MANE Select | ENSP00000364860.3:n.-38del | |
| ENST00000375708.3:c.-38del | ENSP00000364860.3:n.-38del | |
| NM_004560.3:c.-38del | NP_004551.2:n.-38del | |
| NM_001318204.1:c.-38del | NP_001305133.1:n.-38del | |
| XR_001746315.1:n.206del | ||
| NM_004560.4:c.-38del MANE Select | NP_004551.2:n.-38del | |
| NM_001318204.2:c.-38del | NP_001305133.1:n.-38del |