Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154571526C>G , CM000663.2:g.154571526C>G | GRCh38 |
| NC_000001.10:g.154544002C>G , CM000663.1:g.154544002C>G | GRCh37 |
| NC_000001.9:g.152810626C>G | NCBI36 |
| NG_008027.1:g.8746C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.703C>G MANE Select | ENSP00000357461.3:p.Leu235Val | |
| ENST00000636034.1:c.703C>G | ENSP00000489703.1:p.Leu235Val | |
| ENST00000637900.1:c.709C>G | ENSP00000490474.1:p.Leu237Val | |
| ENST00000368476.3:c.703C>G | ENSP00000357461.3:p.Leu235Val | |
| NM_000748.2:c.703C>G | NP_000739.1:p.Leu235Val | |
| XM_017000180.2:c.193C>G | XP_016855669.1:p.Leu65Val | |
| XR_001736952.2:n.955C>G | ||
| NM_000748.3:c.703C>G MANE Select | NP_000739.1:p.Leu235Val |