Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118312627T>A , CM000673.2:g.118312627T>A | GRCh38 |
| NC_000011.9:g.118183342T>A , CM000673.1:g.118183342T>A | GRCh37 |
| NC_000011.8:g.117688552T>A | NCBI36 |
| NG_007383.1:g.13048T>A , LRG_38:g.13048T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361763.9:c.113T>A MANE Select | ENSP00000354566.4:p.Val38Asp | |
| ENST00000361763.8:c.113T>A | ENSP00000354566.4:p.Val38Asp | |
| ENST00000526146.5:n.659T>A | ||
| ENST00000528435.5:n.666T>A | ||
| ENST00000528600.1:c.95T>A | ENSP00000433975.1:p.Val32Asp | |
| ENST00000529713.5:n.219T>A | ||
| ENST00000531913.1:n.484T>A | ||
| NM_000733.3:c.113T>A , LRG_38t1:c.113T>A | NP_000724.1:p.Val38Asp | |
| NM_000733.4:c.113T>A MANE Select | NP_000724.1:p.Val38Asp |