Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18785789C= , CM000681.2:g.18785789C= | GRCh38 |
| NC_000019.9:g.18896599C= , CM000681.1:g.18896599C= | GRCh37 |
| NC_000019.8:g.18757599C= | NCBI36 |
| NG_007070.1:g.10516G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.1552G= MANE Select | ENSP00000222271.2:p.Asp518= | |
| ENST00000222271.6:c.1552G= | ENSP00000222271.2:p.Asp518= | |
| ENST00000425807.1:c.1393G= | ENSP00000403792.1:p.Asp465= | |
| ENST00000542601.6:c.1453G= | ENSP00000439156.2:p.Asp485= | |
| NM_000095.2:c.1552G= | NP_000086.2:p.Asp518= | |
| NM_000095.3:c.1552G= MANE Select | NP_000086.2:p.Asp518= |