Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116822773T>A , CM000673.2:g.116822773T>A | GRCh38 |
| NC_000011.9:g.116693489T>A , CM000673.1:g.116693489T>A | GRCh37 |
| NC_000011.8:g.116198699T>A | NCBI36 |
| NG_012044.1:g.5523A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357780.5:c.62A>T MANE Select | ENSP00000350425.3:p.Glu21Val | |
| ENST00000357780.4:c.62A>T | ENSP00000350425.3:p.Glu21Val | |
| NM_000482.3:c.62A>T | NP_000473.2:p.Glu21Val | |
| NM_000482.4:c.62A>T MANE Select | NP_000473.2:p.Glu21Val |