Linked Data
gnomAD v4:
20-34280222-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.34280222T>G , CM000682.2:g.34280222T>G | GRCh38 |
| NC_000020.10:g.32868028T>G , CM000682.1:g.32868028T>G | GRCh37 |
| NC_000020.9:g.32331689T>G | NCBI36 |
| NG_012630.1:g.36581A>C | |
| NG_012630.2:g.36581A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011528657.1:c.*7+805A>C | XP_011526959.1:n.*7+805A>C | |
| XM_011528658.1:c.*7+805A>C | XP_011526960.1:n.*7+805A>C | |
| XM_011528657.2:c.*7+805A>C | XP_011526959.2:n.*7+805A>C | |
| XM_011528658.3:c.*7+805A>C | XP_011526960.2:n.*7+805A>C | |
| XM_017027709.2:c.*7+805A>C | XP_016883198.1:n.*7+805A>C |