Linked Data
gnomAD v4:
6-29946020-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29946021del , CM000668.2:g.29946021del | GRCh38 |
| NC_000006.11:g.29913798del , CM000668.1:g.29913798del | GRCh37 |
| NC_000006.10:g.30021777del | NCBI36 |
| NG_029217.2:g.8557del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706901.1:c.*566del | ENSP00000516612.1:n.*566del | |
| ENST00000706902.1:c.1093+740del | ENSP00000516613.1:n.1093+740del | |
| ENST00000706903.1:c.*124+442del | ENSP00000516614.1:n.*124+442del | |
| ENST00000706904.1:c.1093+740del | ENSP00000516615.1:n.1093+740del | |
| ENST00000706905.1:c.*566del | ENSP00000516616.1:n.*566del |