Linked Data
dbSNP Id:
rs34740366
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226579T>A , CM000673.2:g.5226579T>A | GRCh38 |
| NC_000011.9:g.5247809T>A , CM000673.1:g.5247809T>A | GRCh37 |
| NC_000011.8:g.5204385T>A | NCBI36 |
| NG_000007.3:g.71037A>T | |
| NG_059281.1:g.5493A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647020.1:c.313A>T | ENSP00000494175.1:p.Arg105Trp | |
| ENST00000335295.4:c.313A>T MANE Select | ENSP00000333994.3:p.Arg105Trp | |
| ENST00000475226.1:n.245A>T | ||
| ENST00000485743.1:n.364A>T | ||
| ENST00000633227.1:c.*129A>T | ENSP00000488004.1:n.*129A>T | |
| NM_000518.4:c.313A>T | NP_000509.1:p.Arg105Trp | |
| NM_000518.5:c.313A>T MANE Select | NP_000509.1:p.Arg105Trp |