Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.58782482A>T , CM000663.2:g.58782482A>T | GRCh38 |
| NC_000001.10:g.59248154A>T , CM000663.1:g.59248154A>T | GRCh37 |
| NC_000001.9:g.59020742A>T | NCBI36 |
| NG_047027.1:g.6632T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710273.1:c.655T>A | ENSP00000518166.1:p.Phe219Ile | |
| ENST00000371222.4:c.589T>A MANE Select | ENSP00000360266.2:p.Phe197Ile | |
| ENST00000678696.1:c.589T>A | ENSP00000503132.1:p.Phe197Ile | |
| ENST00000371222.3:c.589T>A | ENSP00000360266.2:p.Phe197Ile | |
| NM_002228.3:c.589T>A | NP_002219.1:p.Phe197Ile | |
| NM_002228.4:c.589T>A MANE Select | NP_002219.1:p.Phe197Ile |