Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45984309G>A , CM000683.2:g.45984309G>A | GRCh38 |
| NC_000021.8:g.47404223G>A , CM000683.1:g.47404223G>A | GRCh37 |
| NC_000021.7:g.46228651G>A | NCBI36 |
| NG_008674.1:g.7561G>A , LRG_475:g.7561G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001848.3:c.268G>A MANE Select | NP_001839.2:p.Ala90Thr |
| ENST00000361866.8:c.268G>A MANE Select | ENSP00000355180.3:p.Ala90Thr |
| NM_001848.2:c.268G>A , LRG_475t1:c.268G>A | NP_001839.2:p.Ala90Thr |
| ENST00000361866.7:c.268G>A | ENSP00000355180.3:p.Ala90Thr |
| ENST00000612273.1:c.268G>A | ENSP00000483630.1:p.Ala90Thr |