Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.84840502G= , CM000677.2:g.84840502G= | GRCh38 |
| NC_000015.9:g.85383733G= , CM000677.1:g.85383733G= | GRCh37 |
| NC_000015.8:g.83184737G= | NCBI36 |
| NG_054748.1:g.28872G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258888.6:c.1223G= MANE Select | ENSP00000258888.6:p.Gly408= | |
| ENST00000258888.5:c.1829G= | ENSP00000258888.5:p.Gly610= | |
| NM_020778.4:c.1829G= | NP_065829.3:p.Gly610= | |
| NM_020778.5:c.1223G= MANE Select | NP_065829.4:p.Gly408= |