Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107702050T= , CM000669.2:g.107702050T= | GRCh38 |
| NC_000007.13:g.107342495T= , CM000669.1:g.107342495T= | GRCh37 |
| NC_000007.12:g.107129731T= | NCBI36 |
| NG_008489.1:g.46416T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.2027T= MANE Select | ENSP00000494017.1:p.Leu676= | |
| ENST00000644846.1:c.738T= | ||
| ENST00000265715.7:c.2027T= | ENSP00000265715.3:p.Leu676= | |
| ENST00000492030.2:n.314T= | ||
| NM_000441.1:c.2027T= | NP_000432.1:p.Leu676= | |
| XM_005250425.1:c.2027T= | XP_005250482.1:p.Leu676= | |
| XM_005250425.2:c.2027T= | XP_005250482.1:p.Leu676= | |
| XM_017012318.1:c.1949T= | XP_016867807.1:p.Leu650= | |
| NM_000441.2:c.2027T= MANE Select | NP_000432.1:p.Leu676= |