Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11965492T>A , CM000663.2:g.11965492T>A | GRCh38 |
| NC_000001.10:g.12025549T>A , CM000663.1:g.12025549T>A | GRCh37 |
| NC_000001.9:g.11948136T>A | NCBI36 |
| NG_008159.1:g.35804T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000196061.5:c.1483T>A MANE Select | ENSP00000196061.4:p.Phe495Ile | |
| ENST00000196061.4:c.1483T>A | ENSP00000196061.4:p.Phe495Ile | |
| ENST00000470133.1:n.97T>A | ||
| ENST00000491536.5:n.111T>A | ||
| NM_000302.3:c.1483T>A | NP_000293.2:p.Phe495Ile | |
| NM_001316320.1:c.1624T>A | NP_001303249.1:p.Phe542Ile | |
| XM_011541594.1:c.1564T>A | XP_011539896.1:p.Phe522Ile | |
| XM_024447707.1:c.817T>A | XP_024303475.1:p.Phe273Ile | |
| NM_000302.4:c.1483T>A MANE Select | NP_000293.2:p.Phe495Ile | |
| NM_001316320.2:c.1624T>A | NP_001303249.1:p.Phe542Ile |