Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.72124176A>T , CM000679.2:g.72124176A>T | GRCh38 |
| NC_000017.10:g.70120317A>T , CM000679.1:g.70120317A>T | GRCh37 |
| NC_000017.9:g.67631912A>T | NCBI36 |
| NG_012490.1:g.8157A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000245479.3:c.1319A>T MANE Select | ENSP00000245479.2:p.Tyr440Phe | |
| ENST00000245479.2:c.1319A>T | ENSP00000245479.2:p.Tyr440Phe | |
| NM_000346.3:c.1319A>T | NP_000337.1:p.Tyr440Phe | |
| NM_000346.4:c.1319A>T MANE Select | NP_000337.1:p.Tyr440Phe |