HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47582351C>T , CM000673.2:g.47582351C>T | GRCh38 |
NC_000011.9:g.47603903C>T , CM000673.1:g.47603903C>T | GRCh37 |
NC_000011.8:g.47560479C>T | NCBI36 |
NG_011946.1:g.8342C>T | |
NG_011946.2:g.8342C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263774.9:c.510C>T MANE Select | ENSP00000263774.4:p.Ile170= | |
ENST00000531351.2:n.1705C>T | ||
ENST00000677462.1:n.2984C>T | ||
ENST00000678975.1:n.2767C>T | ||
ENST00000263774.8:c.510C>T | ENSP00000263774.4:p.Ile170= | |
ENST00000524568.1:n.613C>T | ||
ENST00000525212.1:n.165C>T | ||
ENST00000525378.5:n.448C>T | ||
ENST00000527178.1:n.110C>T | ||
ENST00000533507.5:n.1404C>T | ||
NM_004551.2:c.510C>T | NP_004542.1:p.Ile170= | |
NM_004551.3:c.510C>T MANE Select | NP_004542.1:p.Ile170= |