Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.34857366C>T , CM000668.2:g.34857366C>T | GRCh38 |
| NC_000006.11:g.34825143C>T , CM000668.1:g.34825143C>T | GRCh37 |
| NC_000006.10:g.34933121C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000192788.6:c.1469C>T MANE Select | ENSP00000192788.5:p.Thr490Ile | |
| ENST00000192788.5:c.1469C>T | ENSP00000192788.5:p.Thr490Ile | |
| ENST00000452449.6:c.1469C>T | ENSP00000400628.2:p.Thr490Ile | |
| NM_017754.3:c.1469C>T | NP_060224.3:p.Thr490Ile | |
| XM_005249199.3:c.311C>T | XP_005249256.1:p.Thr104Ile | |
| XM_006715126.2:c.1469C>T | XP_006715189.1:p.Thr490Ile | |
| XM_011514714.1:c.1382C>T | XP_011513016.1:p.Thr461Ile | |
| XM_011514715.1:c.473C>T | XP_011513017.1:p.Thr158Ile | |
| NM_017754.4:c.1469C>T MANE Select | NP_060224.3:p.Thr490Ile |