Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218812728T>A , CM000664.2:g.218812728T>A | GRCh38 |
| NC_000002.11:g.219677451T>A , CM000664.1:g.219677451T>A | GRCh37 |
| NC_000002.10:g.219385695T>A | NCBI36 |
| NG_007959.1:g.35980T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.823T>A MANE Select | ENSP00000258415.4:p.Trp275Arg | |
| ENST00000258415.8:c.823T>A | ENSP00000258415.4:p.Trp275Arg | |
| ENST00000411688.1:c.541T>A | ENSP00000392671.1:p.Trp181Arg | |
| ENST00000445971.1:c.*284T>A | ENSP00000404945.1:n.*284T>A | |
| ENST00000466602.1:n.771T>A | ||
| ENST00000494263.5:n.1257T>A | ||
| NM_000784.3:c.823T>A | NP_000775.1:p.Trp275Arg | |
| XM_017003488.2:c.403T>A | XP_016858977.1:p.Trp135Arg | |
| NM_000784.4:c.823T>A MANE Select | NP_000775.1:p.Trp275Arg |