Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55151884T= , CM000681.2:g.55151884T= | GRCh38 |
| NC_000019.9:g.55663252T= , CM000681.1:g.55663252T= | GRCh37 |
| NC_000019.8:g.60355064T= | NCBI36 |
| NG_007866.2:g.10849A= , LRG_432:g.10849A= | |
| NG_011829.2:g.2355A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.583A= MANE Select | ENSP00000341838.5:p.Ile195= | |
| ENST00000665070.1:c.616A= | ENSP00000499482.1:p.Ile206= | |
| ENST00000344887.9:c.583A= | ENSP00000341838.5:p.Ile195= | |
| ENST00000585806.5:n.582A= | ||
| ENST00000588882.1:c.508A= | ENSP00000466729.1:p.Ile170= | |
| ENST00000589864.1:n.411A= | ||
| NM_000363.4:c.583A= , LRG_432t1:c.583A= | NP_000354.4:p.Ile195= | |
| NM_000363.5:c.583A= MANE Select | NP_000354.4:p.Ile195= |