Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19962165C>T , CM000670.2:g.19962165C>T | GRCh38 |
| NC_000008.10:g.19819676C>T , CM000670.1:g.19819676C>T | GRCh37 |
| NC_000008.9:g.19863956C>T | NCBI36 |
| NG_008855.1:g.28095C>T | |
| NG_008855.2:g.65449C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.1373C>T MANE Select | ENSP00000497642.1:p.Ala458Val | |
| ENST00000650478.1:c.313C>T | ENSP00000497560.1:n.313C>T | |
| ENST00000311322.8:c.1373C>T | ENSP00000309757.6:p.Ala458Val | |
| NM_000237.2:c.1373C>T | NP_000228.1:p.Ala458Val | |
| NM_000237.3:c.1373C>T MANE Select | NP_000228.1:p.Ala458Val |