HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47582358A>T , CM000673.2:g.47582358A>T | GRCh38 |
NC_000011.9:g.47603910A>T , CM000673.1:g.47603910A>T | GRCh37 |
NC_000011.8:g.47560486A>T | NCBI36 |
NG_011946.1:g.8349A>T | |
NG_011946.2:g.8349A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263774.9:c.517A>T MANE Select | ENSP00000263774.4:p.Met173Leu | |
ENST00000531351.2:n.1712A>T | ||
ENST00000677462.1:n.2991A>T | ||
ENST00000678975.1:n.2774A>T | ||
ENST00000263774.8:c.517A>T | ENSP00000263774.4:p.Met173Leu | |
ENST00000524568.1:n.620A>T | ||
ENST00000525212.1:n.172A>T | ||
ENST00000525378.5:n.455A>T | ||
ENST00000527178.1:n.117A>T | ||
ENST00000533507.5:n.1411A>T | ||
NM_004551.2:c.517A>T | NP_004542.1:p.Met173Leu | |
NM_004551.3:c.517A>T MANE Select | NP_004542.1:p.Met173Leu |