Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38675853A>G , CM000685.2:g.38675853A>G | GRCh38 |
| NC_000023.10:g.38535107A>G , CM000685.1:g.38535107A>G | GRCh37 |
| NC_000023.9:g.38420051A>G | NCBI36 |
| NG_009160.1:g.119377A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378482.7:c.590A>G MANE Select | ENSP00000367743.2:p.Asn197Ser | |
| ENST00000286824.6:c.641A>G | ENSP00000286824.6:p.Asn214Ser | |
| ENST00000378482.6:c.590A>G | ENSP00000367743.2:p.Asn197Ser | |
| ENST00000419600.3:n.534A>G | ||
| ENST00000465127.1:c.680A>G | ENSP00000417050.1:p.Asn227Ser | |
| ENST00000471410.5:c.*616A>G | ENSP00000419290.1:n.*616A>G | |
| ENST00000475216.5:c.*583A>G | ENSP00000418586.1:n.*583A>G | |
| NM_004615.3:c.590A>G | NP_004606.2:p.Asn197Ser | |
| NM_004615.4:c.590A>G MANE Select | NP_004606.2:p.Asn197Ser |