Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6640182G>A , CM000673.2:g.6640182G>A | GRCh38 |
| NC_000011.9:g.6661413G>A , CM000673.1:g.6661413G>A | GRCh37 |
| NC_000011.8:g.6617989G>A | NCBI36 |
| NG_033858.1:g.20668C>T | |
| NG_033858.2:g.20668C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299441.5:c.1432C>T MANE Select | ENSP00000299441.3:p.Arg478Ter | |
| ENST00000299441.4:c.1432C>T | ENSP00000299441.3:p.Arg478Ter | |
| NM_003737.3:c.1432C>T | NP_003728.1:p.Arg478Ter | |
| NM_003737.4:c.1432C>T MANE Select | NP_003728.1:p.Arg478Ter |