Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.43417613C= , CM000683.2:g.43417613C= | GRCh38 |
| NG_052009.1:g.14520G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_173354.5:c.1906G= MANE Select | NP_775490.2:p.Gly636= |
| ENST00000270162.8:c.1906G= MANE Select | ENSP00000270162.6:p.Gly636= |
| NM_173354.3:c.1906G= | NP_775490.2:p.Gly636= |
| NM_173354.4:c.1906G= | NP_775490.2:p.Gly636= |
| ENST00000270162.6:c.1906G= | ENSP00000270162.6:p.Gly636= |
| XM_011529474.1:c.1759G= | XP_011527776.1:p.Gly587= |
| XM_011529474.2:c.1759G= | XP_011527776.1:p.Gly587= |