Linked Data
gnomAD v4:
15-74749934-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74749934T>A , CM000677.2:g.74749934T>A | GRCh38 |
| NC_000015.9:g.75042275T>A , CM000677.1:g.75042275T>A | GRCh37 |
| NC_000015.8:g.72829328T>A | NCBI36 |
| NG_008431.1:g.32393T>A | |
| NG_008431.2:g.32393T>A | |
| NG_061543.1:g.6090T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.196T>A MANE Select | ENSP00000342007.4:p.Ser66Thr | |
| ENST00000343932.4:c.196T>A | ENSP00000342007.4:p.Ser66Thr | |
| NM_000761.4:c.196T>A | NP_000752.2:p.Ser66Thr | |
| NM_000761.5:c.196T>A MANE Select | NP_000752.2:p.Ser66Thr |