Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.80152837T>G , CM000677.2:g.80152837T>G | GRCh38 |
| NC_000015.9:g.80445179T>G , CM000677.1:g.80445179T>G | GRCh37 |
| NC_000015.8:g.78232234T>G | NCBI36 |
| NG_012833.1:g.4839T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000558767.6:c.-218T>G | ENSP00000507680.1:n.-218T>G | |
| ENST00000261755.9:c.-34T>G | ENSP00000261755.5:n.-34T>G | |
| ENST00000407106.5:c.-98T>G | ENSP00000385080.1:n.-98T>G | |
| ENST00000537726.5:n.49T>G | ||
| ENST00000558022.5:c.-29-189T>G | ENSP00000453152.1:n.-29-189T>G | |
| ENST00000558767.5:n.44T>G | ||
| XM_024449872.1:c.-98T>G | XP_024305640.1:n.-98T>G | |
| NM_001374377.1:c.-98T>G | NP_001361306.1:n.-98T>G | |
| NM_001374380.1:c.-34T>G | NP_001361309.1:n.-34T>G |