Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31598653T>A , CM000680.2:g.31598653T>A | GRCh38 |
| NC_000018.9:g.29178616T>A , CM000680.1:g.29178616T>A | GRCh37 |
| NC_000018.8:g.27432614T>A | NCBI36 |
| NG_009490.1:g.11887T>A , LRG_416:g.11887T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000237014.8:c.422T>A MANE Select | ENSP00000237014.4:p.Val141Asp | |
| ENST00000610404.5:c.326T>A | ENSP00000477599.2:p.Val109Asp | |
| ENST00000649620.1:c.422T>A | ENSP00000497927.1:p.Val141Asp | |
| ENST00000237014.7:c.422T>A | ENSP00000237014.3:p.Val141Asp | |
| ENST00000610404.4:c.536T>A | ENSP00000477599.1:p.Val179Asp | |
| ENST00000613781.1:c.398T>A | ENSP00000479174.1:p.Val133Asp | |
| NM_000371.3:c.422T>A , LRG_416t1:c.422T>A | NP_000362.1:p.Val141Asp | |
| NM_000371.4:c.422T>A MANE Select | NP_000362.1:p.Val141Asp |