Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2286743A>T , CM000678.2:g.2286743A>T | GRCh38 |
| NC_000016.9:g.2336744A>T , CM000678.1:g.2336744A>T | GRCh37 |
| NC_000016.8:g.2276745A>T | NCBI36 |
| NG_011790.1:g.59004T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001089.3:c.3229T>A MANE Select | NP_001080.2:p.Phe1077Ile |
| ENST00000301732.10:c.3229T>A MANE Select | ENSP00000301732.5:p.Phe1077Ile |
| NM_001089.2:c.3229T>A | NP_001080.2:p.Phe1077Ile |
| ENST00000301732.9:c.3229T>A | ENSP00000301732.5:p.Phe1077Ile |
| ENST00000382381.7:c.3055T>A | ENSP00000371818.3:p.Phe1019Ile |