Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.21765807C= , CM000680.2:g.21765807C= | GRCh38 |
| NC_000018.9:g.19345768C= , CM000680.1:g.19345768C= | GRCh37 |
| NC_000018.8:g.17599766C= | NCBI36 |
| NG_033272.2:g.65851C= , LRG_759:g.65851C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_020774.4:c.265C= MANE Select | NP_065825.1:p.Arg89= |
| ENST00000261537.7:c.265C= MANE Select | ENSP00000261537.6:p.Arg89= |
| NM_020774.3:c.265C= , LRG_759t1:c.265C= | NP_065825.1:p.Arg89= |
| ENST00000261537.6:c.265C= | ENSP00000261537.6:p.Arg89= |
| ENST00000578646.5:n.203C= | |
| XM_017025874.1:c.265C= | XP_016881363.1:p.Arg89= |
| XM_017025875.1:c.265C= | XP_016881364.1:p.Arg89= |
| XR_935234.1:n.1056C= | |
| XR_935235.1:n.1056C= |