Linked Data
gnomAD v4:
6-29946022-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29946022A>T , CM000668.2:g.29946022A>T | GRCh38 |
| NC_000006.11:g.29913799A>T , CM000668.1:g.29913799A>T | GRCh37 |
| NC_000006.10:g.30021778A>T | NCBI36 |
| NG_029217.2:g.8558A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706901.1:c.*567A>T | ENSP00000516612.1:n.*567A>T | |
| ENST00000706902.1:c.1093+741A>T | ENSP00000516613.1:n.1093+741A>T | |
| ENST00000706903.1:c.*124+443A>T | ENSP00000516614.1:n.*124+443A>T | |
| ENST00000706904.1:c.1093+741A>T | ENSP00000516615.1:n.1093+741A>T | |
| ENST00000706905.1:c.*567A>T | ENSP00000516616.1:n.*567A>T |