Linked Data
gnomAD v4:
6-1613021-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1613022del , CM000668.2:g.1613022del | GRCh38 |
| NC_000006.11:g.1613257del , CM000668.1:g.1613257del | GRCh37 |
| NC_000006.10:g.1558256del | NCBI36 |
| NG_009368.1:g.7577del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645831.2:c.*915del MANE Select | ENSP00000493906.1:n.*915del | |
| ENST00000380874.3:c.*915del | ENSP00000370256.2:n.*915del | |
| NM_001453.2:c.2577del | NP_001444.2:n.2577del | |
| NM_001453.3:c.*915del MANE Select | NP_001444.2:n.*915del |