Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.43420347G= , CM000683.2:g.43420347G= | GRCh38 |
| NG_052009.1:g.11786C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_173354.5:c.859C= MANE Select | NP_775490.2:p.Pro287= |
| ENST00000270162.8:c.859C= MANE Select | ENSP00000270162.6:p.Pro287= |
| NM_173354.3:c.859C= | NP_775490.2:p.Pro287= |
| NM_173354.4:c.859C= | NP_775490.2:p.Pro287= |
| ENST00000270162.6:c.859C= | ENSP00000270162.6:p.Pro287= |
| XM_011529474.1:c.859C= | XP_011527776.1:p.Pro287= |
| XM_011529474.2:c.859C= | XP_011527776.1:p.Pro287= |