Linked Data
gnomAD v4:
20-10673743-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10673747del , CM000682.2:g.10673747del | GRCh38 |
| NC_000020.10:g.10654395del , CM000682.1:g.10654395del | GRCh37 |
| NC_000020.9:g.10602395del | NCBI36 |
| NG_007496.1:g.5303del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.-214del MANE Select | ENSP00000254958.4:n.-214del | |
| ENST00000254958.9:c.-214del | ENSP00000254958.4:n.-214del | |
| NM_000214.2:c.-214del | NP_000205.1:n.-214del | |
| NM_000214.3:c.-214del MANE Select | NP_000205.1:n.-214del |