Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47283364T= , CM000679.2:g.47283364T= | GRCh38 |
| NC_000017.10:g.45360730T= , CM000679.1:g.45360730T= | GRCh37 |
| NC_000017.9:g.42715729T= | NCBI36 |
| NG_008332.2:g.34523T= , LRG_481:g.34523T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696963.1:c.176T= | ENSP00000513002.1:p.Leu59= | |
| ENST00000559488.7:c.176T= MANE Select | ENSP00000452786.2:p.Leu59= | |
| ENST00000559488.5:c.176T= | ENSP00000452786.1:p.Leu59= | |
| ENST00000560629.1:c.141T= | ||
| ENST00000571680.1:c.176T= | ENSP00000461626.1:p.Leu59= | |
| NM_000212.2:c.176T= , LRG_481t1:c.176T= | NP_000203.2:p.Leu59= | |
| NM_000212.3:c.176T= MANE Select | NP_000203.2:p.Leu59= |