Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94989003A>G , CM000672.2:g.94989003A>G | GRCh38 |
| NC_000010.10:g.96748760A>G , CM000672.1:g.96748760A>G | GRCh37 |
| NC_000010.9:g.96738750A>G | NCBI36 |
| NG_008385.1:g.55346A>G | |
| NG_008385.2:g.55846A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.1448A>G MANE Select | ENSP00000260682.6:p.Tyr483Cys | |
| ENST00000643112.1:c.*457A>G | ENSP00000496202.1:n.*457A>G | |
| ENST00000260682.6:c.1448A>G | ENSP00000260682.6:p.Tyr483Cys | |
| NM_000771.3:c.1448A>G | NP_000762.2:p.Tyr483Cys | |
| NM_000771.4:c.1448A>G MANE Select | NP_000762.2:p.Tyr483Cys |