Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89776768C>A , CM000677.2:g.89776768C>A | GRCh38 |
| NC_000015.9:g.90319999C>A , CM000677.1:g.90319999C>A | GRCh37 |
| NC_000015.8:g.88121003C>A | NCBI36 |
| NG_008608.1:g.5411C>A | |
| NG_008608.2:g.21178C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341735.5:c.411C>A MANE Select | ENSP00000342392.3:p.Ala137= | |
| ENST00000341735.3:c.411C>A | ENSP00000342392.3:p.Ala137= | |
| ENST00000558723.1:n.39-1297C>A | ||
| ENST00000560219.2:c.31-1297C>A | ENSP00000452998.1:n.31-1297C>A | |
| NM_001039958.1:c.411C>A | NP_001035047.1:p.Ala137= | |
| NM_001039958.2:c.411C>A MANE Select | NP_001035047.1:p.Ala137= |