Linked Data
gnomAD v4:
17-41586769-GC-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586774del , CM000679.2:g.41586774del | GRCh38 |
| NC_000017.10:g.39743026del , CM000679.1:g.39743026del | GRCh37 |
| NC_000017.9:g.36996552del | NCBI36 |
| NG_008624.1:g.5126del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.65del MANE Select | ENSP00000167586.6:p.Gly22AlafsTer? | |
| ENST00000167586.6:c.65del | ENSP00000167586.6:p.Gly22AlafsTer? | |
| NM_000526.4:c.65del | NP_000517.2:p.Gly22AlafsTer? | |
| NM_000526.5:c.65del MANE Select | NP_000517.3:p.Gly22AlafsTer? |