Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10656451G>T , CM000682.2:g.10656451G>T | GRCh38 |
| NC_000020.10:g.10637099G>T , CM000682.1:g.10637099G>T | GRCh37 |
| NC_000020.9:g.10585099G>T | NCBI36 |
| NG_007496.1:g.22596C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000214.3:c.702C>A MANE Select | NP_000205.1:p.Cys234Ter |
| ENST00000254958.10:c.702C>A MANE Select | ENSP00000254958.4:p.Cys234Ter |
| NM_000214.2:c.702C>A | NP_000205.1:p.Cys234Ter |
| ENST00000254958.9:c.702C>A | ENSP00000254958.4:p.Cys234Ter |
| ENST00000423891.6:n.568C>A |