Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110781075G>A , CM000672.2:g.110781075G>A | GRCh38 |
| NC_000010.10:g.112540833G>A , CM000672.1:g.112540833G>A | GRCh37 |
| NC_000010.9:g.112530823G>A | NCBI36 |
| NG_021177.1:g.141679G>A , LRG_382:g.141679G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369519.4:c.466G>A MANE Select | ENSP00000358532.3:p.Ala156Thr | |
| ENST00000369519.3:c.466G>A | ENSP00000358532.3:p.Ala156Thr | |
| NM_001134363.2:c.466G>A | NP_001127835.2:p.Ala156Thr | |
| XM_011539697.1:c.82G>A | XP_011537999.1:p.Ala28Thr | |
| XM_017016103.2:c.301G>A | XP_016871592.1:p.Ala101Thr | |
| XM_017016104.2:c.82G>A | XP_016871593.1:p.Ala28Thr | |
| NM_001134363.3:c.466G>A MANE Select | NP_001127835.2:p.Ala156Thr |