Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38675826A>T , CM000685.2:g.38675826A>T | GRCh38 |
| NC_000023.10:g.38535080A>T , CM000685.1:g.38535080A>T | GRCh37 |
| NC_000023.9:g.38420024A>T | NCBI36 |
| NG_009160.1:g.119350A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378482.7:c.563A>T MANE Select | ENSP00000367743.2:p.Asn188Ile | |
| ENST00000286824.6:c.614A>T | ENSP00000286824.6:p.Asn205Ile | |
| ENST00000378482.6:c.563A>T | ENSP00000367743.2:p.Asn188Ile | |
| ENST00000419600.3:n.507A>T | ||
| ENST00000465127.1:c.653A>T | ENSP00000417050.1:p.Asn218Ile | |
| ENST00000471410.5:c.*589A>T | ENSP00000419290.1:n.*589A>T | |
| ENST00000475216.5:c.*556A>T | ENSP00000418586.1:n.*556A>T | |
| NM_004615.3:c.563A>T | NP_004606.2:p.Asn188Ile | |
| NM_004615.4:c.563A>T MANE Select | NP_004606.2:p.Asn188Ile |