Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10649544C>T , CM000682.2:g.10649544C>T | GRCh38 |
| NC_000020.10:g.10630192C>T , CM000682.1:g.10630192C>T | GRCh37 |
| NC_000020.9:g.10578192C>T | NCBI36 |
| NG_007496.1:g.29503G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.1326G>A MANE Select | ENSP00000254958.4:p.Trp442Ter | |
| ENST00000617965.2:n.1915G>A | ||
| ENST00000254958.9:c.1326G>A | ENSP00000254958.4:p.Trp442Ter | |
| ENST00000423891.6:n.1192G>A | ||
| ENST00000620743.1:n.45G>A | ||
| ENST00000622545.1:c.103G>A | ||
| NM_000214.2:c.1326G>A | NP_000205.1:p.Trp442Ter | |
| NM_000214.3:c.1326G>A MANE Select | NP_000205.1:p.Trp442Ter |