Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.64759116G>A , CM000674.2:g.64759116G>A | GRCh38 |
| NC_000012.11:g.65152896G>A , CM000674.1:g.65152896G>A | GRCh37 |
| NC_000012.10:g.63439163G>A | NCBI36 |
| NG_008955.1:g.5331C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002076.4:c.161C>T MANE Select | NP_002067.1:p.Thr54Met |
| ENST00000258145.8:c.161C>T MANE Select | ENSP00000258145.3:p.Thr54Met |
| NM_002076.3:c.161C>T | NP_002067.1:p.Thr54Met |
| ENST00000258145.7:c.161C>T | ENSP00000258145.3:p.Thr54Met |
| ENST00000542058.5:c.161C>T | ENSP00000444819.1:p.Thr54Met |
| ENST00000543646.5:c.161C>T | ENSP00000438497.1:p.Thr54Met |