Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218812236G>A , CM000664.2:g.218812236G>A | GRCh38 |
| NC_000002.11:g.219676959G>A , CM000664.1:g.219676959G>A | GRCh37 |
| NC_000002.10:g.219385203G>A | NCBI36 |
| NG_007959.1:g.35488G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000784.4:c.461G>A MANE Select | NP_000775.1:p.Trp154Ter |
| ENST00000258415.9:c.461G>A MANE Select | ENSP00000258415.4:p.Trp154Ter |
| NM_000784.3:c.461G>A | NP_000775.1:p.Trp154Ter |
| ENST00000258415.8:c.461G>A | ENSP00000258415.4:p.Trp154Ter |
| ENST00000411688.1:c.179G>A | ENSP00000392671.1:p.Trp60Ter |
| ENST00000445971.1:c.270G>A | ENSP00000404945.1:p.Leu90= |
| ENST00000466602.1:n.279G>A | |
| ENST00000494263.5:n.895G>A | |
| XM_017003488.2:c.41G>A | XP_016858977.1:p.Trp14Ter |