Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.65029421C= , CM000677.2:g.65029421C= | GRCh38 |
| NC_000015.9:g.65321759C= , CM000677.1:g.65321759C= | GRCh37 |
| NC_000015.8:g.63108812C= | NCBI36 |
| NG_029184.1:g.5219G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000220058.9:c.193G= MANE Select | ENSP00000220058.4:p.Ala65= | |
| ENST00000220058.8:c.193G= | ENSP00000220058.4:p.Ala65= | |
| ENST00000543678.1:c.193G= | ENSP00000443754.1:p.Ala65= | |
| ENST00000558460.5:c.193G= | ENSP00000452646.1:p.Ala65= | |
| ENST00000558614.1:n.154G= | ||
| ENST00000559633.1:n.112G= | ||
| ENST00000560717.5:c.178G= | ENSP00000457257.1:p.Ala60= | |
| NM_139242.3:c.193G= | NP_640335.2:p.Ala65= | |
| XM_005254158.5:c.193G= | XP_005254215.2:p.Ala65= | |
| XR_001751081.1:n.208G= | ||
| NM_139242.4:c.193G= MANE Select | NP_640335.2:p.Ala65= |