Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40161227G>A , CM000677.2:g.40161227G>A | GRCh38 |
| NC_000015.9:g.40453428G>A , CM000677.1:g.40453428G>A | GRCh37 |
| NC_000015.8:g.38240720G>A | NCBI36 |
| NG_016338.1:g.5219G>A , LRG_489:g.5219G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000287598.11:c.7G>A MANE Select | ENSP00000287598.7:p.Ala3Thr | |
| ENST00000287598.10:c.7G>A | ENSP00000287598.6:p.Ala3Thr | |
| ENST00000412359.7:c.7G>A | ENSP00000398470.3:p.Ala3Thr | |
| ENST00000558715.5:c.7G>A | ENSP00000453861.1:p.Ala3Thr | |
| ENST00000559414.5:n.185G>A | ||
| ENST00000560120.5:n.205G>A | ||
| NM_001211.5:c.7G>A , LRG_489t1:c.7G>A | NP_001202.4:p.Ala3Thr | |
| NM_001211.6:c.7G>A MANE Select | NP_001202.5:p.Ala3Thr |