Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10644885C>T , CM000682.2:g.10644885C>T | GRCh38 |
| NC_000020.10:g.10625533C>T , CM000682.1:g.10625533C>T | GRCh37 |
| NC_000020.9:g.10573533C>T | NCBI36 |
| NG_007496.1:g.34162G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000214.3:c.2322G>A MANE Select | NP_000205.1:p.Trp774Ter |
| ENST00000254958.10:c.2322G>A MANE Select | ENSP00000254958.4:p.Trp774Ter |
| NM_000214.2:c.2322G>A | NP_000205.1:p.Trp774Ter |
| ENST00000254958.9:c.2322G>A | ENSP00000254958.4:p.Trp774Ter |
| ENST00000423891.6:n.2188G>A | |
| ENST00000488480.2:n.719G>A | |
| ENST00000617965.2:n.2911G>A |