Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86654023T>A , CM000670.2:g.86654023T>A | GRCh38 |
| NC_000008.10:g.87666251T>A , CM000670.1:g.87666251T>A | GRCh37 |
| NC_000008.9:g.87735367T>A | NCBI36 |
| NG_016980.1:g.94653A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_019098.5:c.892A>T MANE Select | NP_061971.3:p.Thr298Ser |
| ENST00000320005.6:c.892A>T MANE Select | ENSP00000316605.5:p.Thr298Ser |
| NM_019098.4:c.892A>T | NP_061971.3:p.Thr298Ser |
| ENST00000320005.5:c.892A>T | ENSP00000316605.5:p.Thr298Ser |
| ENST00000681546.1:n.712A>T | |
| ENST00000681746.1:c.892A>T | ENSP00000505959.1:p.Thr298Ser |
| XM_011517138.1:c.478A>T | XP_011515440.1:p.Thr160Ser |
| XM_011517138.2:c.478A>T | XP_011515440.1:p.Thr160Ser |