Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4899374T>A , CM000679.2:g.4899374T>A | GRCh38 |
| NC_000017.10:g.4802669T>A , CM000679.1:g.4802669T>A | GRCh37 |
| NC_000017.9:g.4743448T>A | NCBI36 |
| NG_008029.2:g.8702A>T | |
| NG_028005.1:g.71035T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649488.2:c.1043A>T MANE Select | ENSP00000497829.1:p.Glu348Val | |
| ENST00000649830.1:c.110A>T | ENSP00000496907.1:p.Glu37Val | |
| ENST00000652550.1:n.773A>T | ||
| ENST00000293780.4:c.1043A>T | ENSP00000293780.4:p.Glu348Val | |
| ENST00000572438.1:n.729A>T | ||
| NM_000080.3:c.1043A>T | NP_000071.1:p.Glu348Val | |
| NM_000080.4:c.1043A>T MANE Select | NP_000071.1:p.Glu348Val | |
| XM_017024115.1:c.1007A>T | XP_016879604.1:p.Glu336Val | |
| XR_001752421.1:n.1773A>T |