Linked Data
gnomAD v4:
6-29946014-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29946014G>T , CM000668.2:g.29946014G>T | GRCh38 |
| NC_000006.11:g.29913791G>T , CM000668.1:g.29913791G>T | GRCh37 |
| NC_000006.10:g.30021770G>T | NCBI36 |
| NG_029217.2:g.8550G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706901.1:c.*559G>T | ENSP00000516612.1:n.*559G>T | |
| ENST00000706902.1:c.1093+733G>T | ENSP00000516613.1:n.1093+733G>T | |
| ENST00000706903.1:c.*124+435G>T | ENSP00000516614.1:n.*124+435G>T | |
| ENST00000706904.1:c.1093+733G>T | ENSP00000516615.1:n.1093+733G>T | |
| ENST00000706905.1:c.*559G>T | ENSP00000516616.1:n.*559G>T |