Linked Data
gnomAD v4:
6-31270115-TG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31270116del , CM000668.2:g.31270116del | GRCh38 |
| NC_000006.11:g.31237893del , CM000668.1:g.31237893del | GRCh37 |
| NC_000006.10:g.31345872del | NCBI36 |
| NG_029422.2:g.7016del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.896-31del MANE Select | ENSP00000365402.5:n.896-31del | |
| ENST00000376228.9:c.896-31del | ENSP00000365402.5:n.896-31del | |
| ENST00000376237.8:c.*483-31del | ENSP00000365412.4:n.*483-31del | |
| ENST00000383329.7:c.896-31del | ENSP00000372819.3:n.896-31del | |
| ENST00000470363.5:n.214-31del | ||
| ENST00000487245.5:n.1255-31del | ||
| NM_002117.5:c.896-31del | NP_002108.4:n.896-31del | |
| NM_002117.6:c.896-31del MANE Select | NP_002108.4:n.896-31del |