Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218814178A>T , CM000664.2:g.218814178A>T | GRCh38 |
| NC_000002.11:g.219678901A>T , CM000664.1:g.219678901A>T | GRCh37 |
| NC_000002.10:g.219387145A>T | NCBI36 |
| NG_007959.1:g.37430A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.1175A>T MANE Select | ENSP00000258415.4:p.Glu392Val | |
| ENST00000258415.8:c.1175A>T | ENSP00000258415.4:p.Glu392Val | |
| ENST00000494263.5:n.1609A>T | ||
| NM_000784.3:c.1175A>T | NP_000775.1:p.Glu392Val | |
| XM_017003488.2:c.755A>T | XP_016858977.1:p.Glu252Val | |
| NM_000784.4:c.1175A>T MANE Select | NP_000775.1:p.Glu392Val |