Linked Data
gnomAD v4:
6-1613142-AT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1613143del , CM000668.2:g.1613143del | GRCh38 |
| NC_000006.11:g.1613378del , CM000668.1:g.1613378del | GRCh37 |
| NC_000006.10:g.1558377del | NCBI36 |
| NG_009368.1:g.7698del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645831.2:c.*1036del MANE Select | ENSP00000493906.1:n.*1036del | |
| ENST00000380874.3:c.*1036del | ENSP00000370256.2:n.*1036del | |
| NM_001453.2:c.2698del | NP_001444.2:n.2698del | |
| NM_001453.3:c.*1036del MANE Select | NP_001444.2:n.*1036del |