Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38074530C>T , CM000664.2:g.38074530C>T | GRCh38 |
| NC_000002.11:g.38301673C>T , CM000664.1:g.38301673C>T | GRCh37 |
| NC_000002.10:g.38155177C>T | NCBI36 |
| NG_008386.2:g.6572G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000104.4:c.859G>A MANE Select | NP_000095.2:p.Ala287Thr |
| ENST00000610745.5:c.859G>A MANE Select | ENSP00000478561.1:p.Ala287Thr |
| NM_000104.3:c.859G>A | NP_000095.2:p.Ala287Thr |
| ENST00000490576.2:c.859G>A | ENSP00000478839.2:p.Ala287Thr |
| ENST00000494864.1:c.-70-3220G>A | ENSP00000479876.1:n.-70-3220G>A |
| ENST00000610745.4:c.859G>A | ENSP00000478561.1:p.Ala287Thr |
| ENST00000613082.1:n.376-122G>A | |
| ENST00000614273.1:c.859G>A | ENSP00000483678.1:p.Ala287Thr |