Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.227164762C>T , CM000664.2:g.227164762C>T | GRCh38 |
| NC_000002.11:g.228029478C>T , CM000664.1:g.228029478C>T | GRCh37 |
| NC_000002.10:g.227737722C>T | NCBI36 |
| NG_011591.1:g.5198C>T , LRG_230:g.5198C>T | |
| NG_011592.1:g.4798G>A , LRG_231:g.4798G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000091.5:c.36C>T MANE Select | NP_000082.2:p.Leu12= |
| ENST00000396578.8:c.36C>T MANE Select | ENSP00000379823.3:p.Leu12= |
| NM_000091.4:c.36C>T , LRG_230t1:c.36C>T | NP_000082.2:p.Leu12= |
| ENST00000396578.7:c.36C>T | ENSP00000379823.3:p.Leu12= |
| XM_005246276.2:c.36C>T | XP_005246333.1:p.Leu12= |
| XM_005246277.2:c.36C>T | XP_005246334.1:p.Leu12= |
| XM_005246277.3:c.36C>T | XP_005246334.1:p.Leu12= |
| XM_005246280.2:c.36C>T | XP_005246337.1:p.Leu12= |
| XM_005246280.3:c.36C>T | XP_005246337.1:p.Leu12= |
| XM_006712245.2:c.36C>T | XP_006712308.1:p.Leu12= |
| XM_006712245.3:c.36C>T | XP_006712308.1:p.Leu12= |
| XM_011510555.1:c.36C>T | XP_011508857.1:p.Leu12= |
| XM_017003295.1:c.36C>T | XP_016858784.1:p.Leu12= |
| XR_001738601.1:n.174C>T | |
| XR_241280.2:n.174C>T | |
| XR_241280.3:n.174C>T |