Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.84840484C= , CM000677.2:g.84840484C= | GRCh38 |
| NC_000015.9:g.85383715C= , CM000677.1:g.85383715C= | GRCh37 |
| NC_000015.8:g.83184719C= | NCBI36 |
| NG_054748.1:g.28854C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258888.6:c.1205C= MANE Select | ENSP00000258888.6:p.Ala402= | |
| ENST00000258888.5:c.1811C= | ENSP00000258888.5:p.Ala604= | |
| NM_020778.4:c.1811C= | NP_065829.3:p.Ala604= | |
| NM_020778.5:c.1205C= MANE Select | NP_065829.4:p.Ala402= |