Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218812707T>A , CM000664.2:g.218812707T>A | GRCh38 |
| NC_000002.11:g.219677430T>A , CM000664.1:g.219677430T>A | GRCh37 |
| NC_000002.10:g.219385674T>A | NCBI36 |
| NG_007959.1:g.35959T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000784.4:c.802T>A MANE Select | NP_000775.1:p.Trp268Arg |
| ENST00000258415.9:c.802T>A MANE Select | ENSP00000258415.4:p.Trp268Arg |
| NM_000784.3:c.802T>A | NP_000775.1:p.Trp268Arg |
| ENST00000258415.8:c.802T>A | ENSP00000258415.4:p.Trp268Arg |
| ENST00000411688.1:c.520T>A | ENSP00000392671.1:p.Trp174Arg |
| ENST00000445971.1:c.*263T>A | ENSP00000404945.1:n.*263T>A |
| ENST00000466602.1:n.750T>A | |
| ENST00000494263.5:n.1236T>A | |
| XM_017003488.2:c.382T>A | XP_016858977.1:p.Trp128Arg |