Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12717791T>A , CM000674.2:g.12717791T>A | GRCh38 |
| NC_000012.11:g.12870725T>A , CM000674.1:g.12870725T>A | GRCh37 |
| NC_000012.10:g.12761992T>A | NCBI36 |
| NG_016341.1:g.5424T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614874.2:c.-49T>A | ENSP00000507272.1:n.-49T>A | |
| ENST00000682620.1:n.1631-1034T>A | ||
| ENST00000684771.1:n.585-1034T>A | ||
| ENST00000228872.9:c.-49T>A MANE Select | ENSP00000228872.4:n.-49T>A | |
| ENST00000228872.8:c.-49T>A | ENSP00000228872.4:n.-49T>A | |
| ENST00000477087.1:n.155-1034T>A | ||
| NM_004064.4:c.-49T>A | NP_004055.1:n.-49T>A | |
| NM_004064.5:c.-49T>A MANE Select | NP_004055.1:n.-49T>A |