Linked Data
gnomAD v4:
20-10673775-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10673780del , CM000682.2:g.10673780del | GRCh38 |
| NC_000020.10:g.10654428del , CM000682.1:g.10654428del | GRCh37 |
| NC_000020.9:g.10602428del | NCBI36 |
| NG_007496.1:g.5271del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.-246del MANE Select | ENSP00000254958.4:n.-246del | |
| ENST00000254958.9:c.-246del | ENSP00000254958.4:n.-246del | |
| NM_000214.2:c.-246del | NP_000205.1:n.-246del | |
| NM_000214.3:c.-246del MANE Select | NP_000205.1:n.-246del |