Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.80152859G>T , CM000677.2:g.80152859G>T | GRCh38 |
| NC_000015.9:g.80445201G>T , CM000677.1:g.80445201G>T | GRCh37 |
| NC_000015.8:g.78232256G>T | NCBI36 |
| NG_012833.1:g.4861G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000558767.6:c.-196G>T | ENSP00000507680.1:n.-196G>T | |
| ENST00000261755.9:c.-30+18G>T | ENSP00000261755.5:n.-30+18G>T | |
| ENST00000407106.5:c.-76G>T | ENSP00000385080.1:n.-76G>T | |
| ENST00000537726.5:n.53+18G>T | ||
| ENST00000558022.5:c.-29-167G>T | ENSP00000453152.1:n.-29-167G>T | |
| ENST00000558767.5:n.66G>T | ||
| ENST00000561369.1:n.5G>T | ||
| XM_024449872.1:c.-76G>T | XP_024305640.1:n.-76G>T | |
| NM_001374377.1:c.-76G>T | NP_001361306.1:n.-76G>T | |
| NM_001374380.1:c.-30+18G>T | NP_001361309.1:n.-30+18G>T |