Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.2228848T>A , CM000663.2:g.2228848T>A | GRCh38 |
| NC_000001.10:g.2160287T>A , CM000663.1:g.2160287T>A | GRCh37 |
| NC_000001.9:g.2150147T>A | NCBI36 |
| NG_013084.1:g.5154T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003036.4:c.82T>A MANE Select | NP_003027.1:p.Ser28Thr |
| ENST00000378536.5:c.82T>A MANE Select | ENSP00000367797.4:p.Ser28Thr |
| NM_003036.3:c.82T>A | NP_003027.1:p.Ser28Thr |
| ENST00000378536.4:c.82T>A | ENSP00000367797.4:p.Ser28Thr |
| ENST00000704337.1:n.137+1324T>A | |
| XM_005244775.2:c.82T>A | XP_005244832.1:p.Ser28Thr |
| XM_005244775.3:c.82T>A | XP_005244832.1:p.Ser28Thr |