Linked Data
gnomAD v4:
6-31269015-CG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31269020del , CM000668.2:g.31269020del | GRCh38 |
| NC_000006.11:g.31236797del , CM000668.1:g.31236797del | GRCh37 |
| NC_000006.10:g.31344776del | NCBI36 |
| NG_029422.2:g.8116del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.*153del MANE Select | ENSP00000365402.5:n.*153del | |
| ENST00000376228.9:c.*153del | ENSP00000365402.5:n.*153del | |
| ENST00000376237.8:c.*841del | ENSP00000365412.4:n.*841del | |
| ENST00000383329.7:c.*153del | ENSP00000372819.3:n.*153del | |
| ENST00000466892.5:n.487del | ||
| ENST00000470363.5:n.1012del | ||
| ENST00000487245.5:n.1613del | ||
| NM_002117.5:c.*153del | NP_002108.4:n.*153del | |
| NM_002117.6:c.*153del MANE Select | NP_002108.4:n.*153del |