HGVS | Genome Assembly |
---|---|
NC_000011.10:g.102527662A>C , CM000673.2:g.102527662A>C | GRCh38 |
NC_000011.9:g.102398393A>C , CM000673.1:g.102398393A>C | GRCh37 |
NC_000011.8:g.101903603A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260227.5:c.346T>G MANE Select | ENSP00000260227.4:p.Tyr116Asp | |
ENST00000260227.4:c.346T>G | ENSP00000260227.4:p.Tyr116Asp | |
ENST00000531200.1:n.393T>G | ||
ENST00000533366.5:n.396T>G | ||
NM_002423.3:c.346T>G | NP_002414.1:p.Tyr116Asp | |
NM_002423.4:c.346T>G | NP_002414.1:p.Tyr116Asp | |
NM_002423.5:c.346T>G MANE Select | NP_002414.1:p.Tyr116Asp |