Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.78118152T>A , CM000685.2:g.78118152T>A | GRCh38 |
| NC_000023.10:g.77373649T>A , CM000685.1:g.77373649T>A | GRCh37 |
| NC_000023.9:g.77260305T>A | NCBI36 |
| NG_008862.1:g.18984T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373316.5:c.623T>A MANE Select | ENSP00000362413.4:p.Phe208Tyr | |
| ENST00000644362.1:c.539T>A | ENSP00000496140.1:p.Phe180Tyr | |
| ENST00000373316.4:c.623T>A | ENSP00000362413.4:p.Phe208Tyr | |
| ENST00000491291.1:n.615T>A | ||
| NM_000291.3:c.623T>A | NP_000282.1:p.Phe208Tyr | |
| NM_000291.4:c.623T>A MANE Select | NP_000282.1:p.Phe208Tyr |