Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.60371415G>T , CM000680.2:g.60371415G>T | GRCh38 |
| NC_000018.9:g.58038648G>T , CM000680.1:g.58038648G>T | GRCh37 |
| NC_000018.8:g.56189628G>T | NCBI36 |
| NG_016441.1:g.6354C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299766.5:c.935C>A MANE Select | ENSP00000299766.3:p.Thr312Asn | |
| ENST00000299766.4:c.935C>A | ENSP00000299766.3:p.Thr312Asn | |
| NM_005912.2:c.935C>A | NP_005903.2:p.Thr312Asn | |
| NM_005912.3:c.935C>A MANE Select | NP_005903.2:p.Thr312Asn |