HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47582352T>G , CM000673.2:g.47582352T>G | GRCh38 |
NC_000011.9:g.47603904T>G , CM000673.1:g.47603904T>G | GRCh37 |
NC_000011.8:g.47560480T>G | NCBI36 |
NG_011946.1:g.8343T>G | |
NG_011946.2:g.8343T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000263774.9:c.511T>G MANE Select | ENSP00000263774.4:p.Trp171Gly | |
ENST00000531351.2:n.1706T>G | ||
ENST00000677462.1:n.2985T>G | ||
ENST00000678975.1:n.2768T>G | ||
ENST00000263774.8:c.511T>G | ENSP00000263774.4:p.Trp171Gly | |
ENST00000524568.1:n.614T>G | ||
ENST00000525212.1:n.166T>G | ||
ENST00000525378.5:n.449T>G | ||
ENST00000527178.1:n.111T>G | ||
ENST00000533507.5:n.1405T>G | ||
NM_004551.2:c.511T>G | NP_004542.1:p.Trp171Gly | |
NM_004551.3:c.511T>G MANE Select | NP_004542.1:p.Trp171Gly |