Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.21741710G= , CM000680.2:g.21741710G= | GRCh38 |
| NC_000018.9:g.19321671G= , CM000680.1:g.19321671G= | GRCh37 |
| NC_000018.8:g.17575669G= | NCBI36 |
| NG_033272.2:g.41754G= , LRG_759:g.41754G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_020774.4:c.127G= MANE Select | NP_065825.1:p.Glu43= |
| ENST00000261537.7:c.127G= MANE Select | ENSP00000261537.6:p.Glu43= |
| NM_020774.3:c.127G= , LRG_759t1:c.127G= | NP_065825.1:p.Glu43= |
| ENST00000261537.6:c.127G= | ENSP00000261537.6:p.Glu43= |
| ENST00000578646.5:n.168-24062G= | |
| XM_017025874.1:c.127G= | XP_016881363.1:p.Glu43= |
| XM_017025875.1:c.127G= | XP_016881364.1:p.Glu43= |
| XR_935234.1:n.918G= | |
| XR_935235.1:n.918G= |