Linked Data
gnomAD v4:
20-10673537-GC-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10673539del , CM000682.2:g.10673539del | GRCh38 |
| NC_000020.10:g.10654187del , CM000682.1:g.10654187del | GRCh37 |
| NC_000020.9:g.10602187del | NCBI36 |
| NG_007496.1:g.5509del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.-8del MANE Select | ENSP00000254958.4:n.-8del | |
| ENST00000254958.9:c.-8del | ENSP00000254958.4:n.-8del | |
| NM_000214.2:c.-8del | NP_000205.1:n.-8del | |
| NM_000214.3:c.-8del MANE Select | NP_000205.1:n.-8del |