Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68670109C= , CM000666.2:g.68670109C= | GRCh38 |
| NC_000004.11:g.69535827C= , CM000666.1:g.69535827C= | GRCh37 |
| NC_000004.10:g.69218422C= | NCBI36 |
| NG_052676.1:g.5668G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338206.6:c.510G= MANE Select | ENSP00000341045.5:p.Leu170= | |
| ENST00000338206.5:c.510G= | ENSP00000341045.5:p.Leu170= | |
| ENST00000616841.4:c.510G= | ENSP00000482004.1:p.Leu170= | |
| NM_001076.3:c.510G= | NP_001067.2:p.Leu170= | |
| NM_001076.4:c.510G= MANE Select | NP_001067.2:p.Leu170= |