Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586361C= , CM000679.2:g.41586361C= | GRCh38 |
| NC_000017.10:g.39742613C= , CM000679.1:g.39742613C= | GRCh37 |
| NC_000017.9:g.36996139C= | NCBI36 |
| NG_008624.1:g.5535G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.474G= MANE Select | ENSP00000167586.6:p.Glu158= | |
| ENST00000167586.6:c.474G= | ENSP00000167586.6:p.Glu158= | |
| NM_000526.4:c.474G= | NP_000517.2:p.Glu158= | |
| NM_000526.5:c.474G= MANE Select | NP_000517.3:p.Glu158= |