Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44289692T>A , CM000683.2:g.44289692T>A | GRCh38 |
| NC_000021.8:g.45709575T>A , CM000683.1:g.45709575T>A | GRCh37 |
| NC_000021.7:g.44534003T>A | NCBI36 |
| NG_009556.1:g.8813T>A , LRG_18:g.8813T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291582.6:c.688T>A MANE Select | ENSP00000291582.5:p.Phe230Ile | |
| ENST00000291582.5:c.688T>A | ENSP00000291582.5:p.Phe230Ile | |
| ENST00000527919.5:n.1421T>A | ||
| ENST00000530812.5:n.2438T>A | ||
| NM_000383.3:c.688T>A | NP_000374.1:p.Phe230Ile | |
| XM_011529551.1:c.688T>A | XP_011527853.1:p.Phe230Ile | |
| NM_000383.4:c.688T>A MANE Select | NP_000374.1:p.Phe230Ile |