Linked Data
gnomAD v4:
15-74755248-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74755248T>G , CM000677.2:g.74755248T>G | GRCh38 |
| NC_000015.9:g.75047589T>G , CM000677.1:g.75047589T>G | GRCh37 |
| NC_000015.8:g.72834642T>G | NCBI36 |
| NG_008431.1:g.37707T>G | |
| NG_008431.2:g.37707T>G | |
| NG_061543.1:g.11404T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.*160T>G MANE Select | ENSP00000342007.4:n.*160T>G | |
| ENST00000343932.4:c.*160T>G | ENSP00000342007.4:n.*160T>G | |
| NM_000761.4:c.*160T>G | NP_000752.2:n.*160T>G | |
| NM_000761.5:c.*160T>G MANE Select | NP_000752.2:n.*160T>G |