Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.227164727A>G , CM000664.2:g.227164727A>G | GRCh38 |
| NC_000002.11:g.228029443A>G , CM000664.1:g.228029443A>G | GRCh37 |
| NC_000002.10:g.227737687A>G | NCBI36 |
| NG_011591.1:g.5163A>G , LRG_230:g.5163A>G | |
| NG_011592.1:g.4833T>C , LRG_231:g.4833T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000091.5:c.1A>G MANE Select | NP_000082.2:p.Met1Val |
| ENST00000396578.8:c.1A>G MANE Select | ENSP00000379823.3:p.Met1Val |
| NM_000091.4:c.1A>G , LRG_230t1:c.1A>G | NP_000082.2:p.Met1Val |
| ENST00000396578.7:c.1A>G | ENSP00000379823.3:p.Met1Val |
| XM_005246276.2:c.1A>G | XP_005246333.1:p.Met1Val |
| XM_005246277.2:c.1A>G | XP_005246334.1:p.Met1Val |
| XM_005246277.3:c.1A>G | XP_005246334.1:p.Met1Val |
| XM_005246280.2:c.1A>G | XP_005246337.1:p.Met1Val |
| XM_005246280.3:c.1A>G | XP_005246337.1:p.Met1Val |
| XM_006712245.2:c.1A>G | XP_006712308.1:p.Met1Val |
| XM_006712245.3:c.1A>G | XP_006712308.1:p.Met1Val |
| XM_011510555.1:c.1A>G | XP_011508857.1:p.Met1Val |
| XM_017003295.1:c.1A>G | XP_016858784.1:p.Met1Val |
| XR_001738601.1:n.139A>G | |
| XR_241280.2:n.139A>G | |
| XR_241280.3:n.139A>G |