Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.46003547C>T , CM000683.2:g.46003547C>T | GRCh38 |
| NC_000021.8:g.47423461C>T , CM000683.1:g.47423461C>T | GRCh37 |
| NC_000021.7:g.46247889C>T | NCBI36 |
| NG_008674.1:g.26799C>T , LRG_475:g.26799C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001848.3:c.2621C>T MANE Select | NP_001839.2:p.Ala874Val |
| ENST00000361866.8:c.2621C>T MANE Select | ENSP00000355180.3:p.Ala874Val |
| NM_001848.2:c.2621C>T , LRG_475t1:c.2621C>T | NP_001839.2:p.Ala874Val |
| ENST00000361866.7:c.2621C>T | ENSP00000355180.3:p.Ala874Val |
| ENST00000463060.6:n.1020C>T | |
| ENST00000486023.1:n.409C>T | |
| ENST00000498614.5:n.855C>T | |
| ENST00000612273.1:c.2615C>T | ENSP00000483630.1:p.Ala872Val |
| ENST00000612273.2:c.747C>T | |
| ENST00000682634.1:c.747C>T |