Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.72123632T= , CM000679.2:g.72123632T= | GRCh38 |
| NC_000017.10:g.70119773T= , CM000679.1:g.70119773T= | GRCh37 |
| NC_000017.9:g.67631368T= | NCBI36 |
| NG_012490.1:g.7613T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000245479.3:c.775T= MANE Select | ENSP00000245479.2:p.Leu259= | |
| ENST00000245479.2:c.775T= | ENSP00000245479.2:p.Leu259= | |
| NM_000346.3:c.775T= | NP_000337.1:p.Leu259= | |
| NM_000346.4:c.775T= MANE Select | NP_000337.1:p.Leu259= |