Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.46003939C>T , CM000683.2:g.46003939C>T | GRCh38 |
| NC_000021.8:g.47423853C>T , CM000683.1:g.47423853C>T | GRCh37 |
| NC_000021.7:g.46248281C>T | NCBI36 |
| NG_008674.1:g.27191C>T , LRG_475:g.27191C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001848.3:c.3013C>T MANE Select | NP_001839.2:p.Arg1005Cys |
| ENST00000361866.8:c.3013C>T MANE Select | ENSP00000355180.3:p.Arg1005Cys |
| NM_001848.2:c.3013C>T , LRG_475t1:c.3013C>T | NP_001839.2:p.Arg1005Cys |
| ENST00000361866.7:c.3013C>T | ENSP00000355180.3:p.Arg1005Cys |
| ENST00000463060.6:n.1412C>T | |
| ENST00000486023.1:n.801C>T | |
| ENST00000498614.5:n.1247C>T | |
| ENST00000612273.1:c.3007C>T | ENSP00000483630.1:p.Arg1003Cys |
| ENST00000612273.2:c.1139C>T | |
| ENST00000682634.1:c.1057+82C>T |