Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218812684G>A , CM000664.2:g.218812684G>A | GRCh38 |
| NC_000002.11:g.219677407G>A , CM000664.1:g.219677407G>A | GRCh37 |
| NC_000002.10:g.219385651G>A | NCBI36 |
| NG_007959.1:g.35936G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000258415.9:c.779G>A MANE Select | ENSP00000258415.4:p.Trp260Ter | |
| ENST00000258415.8:c.779G>A | ENSP00000258415.4:p.Trp260Ter | |
| ENST00000411688.1:c.497G>A | ENSP00000392671.1:p.Trp166Ter | |
| ENST00000445971.1:c.*240G>A | ENSP00000404945.1:n.*240G>A | |
| ENST00000466602.1:n.727G>A | ||
| ENST00000494263.5:n.1213G>A | ||
| NM_000784.3:c.779G>A | NP_000775.1:p.Trp260Ter | |
| XM_017003488.2:c.359G>A | XP_016858977.1:p.Trp120Ter | |
| NM_000784.4:c.779G>A MANE Select | NP_000775.1:p.Trp260Ter |