Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154571595C>G , CM000663.2:g.154571595C>G | GRCh38 |
| NC_000001.10:g.154544071C>G , CM000663.1:g.154544071C>G | GRCh37 |
| NC_000001.9:g.152810695C>G | NCBI36 |
| NG_008027.1:g.8815C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.772C>G MANE Select | ENSP00000357461.3:p.Leu258Val | |
| ENST00000636034.1:c.772C>G | ENSP00000489703.1:p.Leu258Val | |
| ENST00000637900.1:c.778C>G | ENSP00000490474.1:p.Leu260Val | |
| ENST00000368476.3:c.772C>G | ENSP00000357461.3:p.Leu258Val | |
| NM_000748.2:c.772C>G | NP_000739.1:p.Leu258Val | |
| XM_017000180.2:c.262C>G | XP_016855669.1:p.Leu88Val | |
| XR_001736952.2:n.1024C>G | ||
| NM_000748.3:c.772C>G MANE Select | NP_000739.1:p.Leu258Val |