Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.46004003C>T , CM000683.2:g.46004003C>T | GRCh38 |
| NC_000021.8:g.47423917C>T , CM000683.1:g.47423917C>T | GRCh37 |
| NC_000021.7:g.46248345C>T | NCBI36 |
| NG_008674.1:g.27255C>T , LRG_475:g.27255C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001848.3:c.3077C>T MANE Select | NP_001839.2:p.Ala1026Val |
| ENST00000361866.8:c.3077C>T MANE Select | ENSP00000355180.3:p.Ala1026Val |
| NM_001848.2:c.3077C>T , LRG_475t1:c.3077C>T | NP_001839.2:p.Ala1026Val |
| ENST00000361866.7:c.3077C>T | ENSP00000355180.3:p.Ala1026Val |
| ENST00000486023.1:n.865C>T | |
| ENST00000498614.5:n.1311C>T | |
| ENST00000612273.1:c.3071C>T | ENSP00000483630.1:p.Ala1024Val |
| ENST00000612273.2:c.1198+5C>T | |
| ENST00000682634.1:c.1057+146C>T |