Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39665871T>G , CM000679.2:g.39665871T>G | GRCh38 |
| NC_000017.10:g.37822124T>G , CM000679.1:g.37822124T>G | GRCh37 |
| NC_000017.9:g.35075650T>G | NCBI36 |
| NG_008892.1:g.5526T>G , LRG_210:g.5526T>G | |
| NG_042278.1:g.2891T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309889.3:c.266T>G MANE Select | ENSP00000312624.2:p.Leu89Arg | |
| ENST00000309889.2:c.266T>G | ENSP00000312624.2:p.Leu89Arg | |
| ENST00000578283.1:c.194T>G | ENSP00000462787.1:p.Leu65Arg | |
| NM_003673.3:c.266T>G , LRG_210t1:c.266T>G | NP_003664.1:p.Leu89Arg | |
| NM_003673.4:c.266T>G MANE Select | NP_003664.1:p.Leu89Arg |