Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3225490T>A , CM000668.2:g.3225490T>A | GRCh38 |
| NC_000006.11:g.3225724T>A , CM000668.1:g.3225724T>A | GRCh37 |
| NC_000006.10:g.3170723T>A | NCBI36 |
| NG_016715.1:g.7245A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259818.8:c.599A>T MANE Select | ENSP00000259818.6:p.Tyr200Phe | |
| ENST00000680070.1:n.1529A>T | ||
| ENST00000681707.1:n.1426A>T | ||
| ENST00000681757.1:n.904A>T | ||
| ENST00000259818.7:c.599A>T | ENSP00000259818.6:p.Tyr200Phe | |
| ENST00000473006.1:n.716A>T | ||
| NM_178012.4:c.599A>T | NP_821080.1:p.Tyr200Phe | |
| XM_011514571.1:c.383A>T | XP_011512873.1:p.Tyr128Phe | |
| NM_178012.5:c.599A>T MANE Select | NP_821080.1:p.Tyr200Phe |