Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154084C>A , CM000681.2:g.55154084C>A | GRCh38 |
| NC_000019.9:g.55665452C>A , CM000681.1:g.55665452C>A | GRCh37 |
| NC_000019.8:g.60357264C>A | NCBI36 |
| NG_007866.2:g.8649G>T , LRG_432:g.8649G>T | |
| NG_011829.2:g.155G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.495G>T MANE Select | ENSP00000341838.5:p.Glu165Asp | |
| ENST00000665070.1:c.528G>T | ENSP00000499482.1:p.Glu176Asp | |
| ENST00000344887.9:c.495G>T | ENSP00000341838.5:p.Glu165Asp | |
| ENST00000585806.5:n.494G>T | ||
| ENST00000588882.1:c.420G>T | ENSP00000466729.1:p.Glu140Asp | |
| ENST00000589864.1:n.323G>T | ||
| NM_000363.4:c.495G>T , LRG_432t1:c.495G>T | NP_000354.4:p.Glu165Asp | |
| NM_000363.5:c.495G>T MANE Select | NP_000354.4:p.Glu165Asp |