Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.180659577C>T , CM000665.2:g.180659577C>T | GRCh38 |
| NC_000003.11:g.180377365C>T , CM000665.1:g.180377365C>T | GRCh37 |
| NC_000003.10:g.181860059C>T | NCBI36 |
| NG_029581.1:g.24919G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000476379.6:c.613G>A MANE Select | ENSP00000417960.2:p.Glu205Lys | |
| ENST00000650641.1:n.692G>A | ||
| ENST00000650889.1:n.785G>A | ||
| ENST00000651046.1:c.613G>A | ENSP00000499175.1:p.Glu205Lys | |
| ENST00000651818.1:n.755G>A | ||
| ENST00000652024.1:n.704G>A | ||
| ENST00000652408.1:n.750G>A | ||
| ENST00000442201.6:c.613G>A | ENSP00000405708.2:p.Glu205Lys | |
| ENST00000476379.5:c.613G>A | ENSP00000417960.1:p.Glu205Lys | |
| NM_181426.1:c.613G>A | NP_852091.1:p.Glu205Lys | |
| NM_181426.2:c.613G>A MANE Select | NP_852091.1:p.Glu205Lys |