HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47582047G= , CM000673.2:g.47582047G= | GRCh38 |
NC_000011.9:g.47603599G= , CM000673.1:g.47603599G= | GRCh37 |
NC_000011.8:g.47560175G= | NCBI36 |
NG_011946.1:g.8038G= | |
NG_011946.2:g.8038G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000263774.9:c.382-41G= MANE Select | ENSP00000263774.4:n.382-41G= | |
ENST00000531351.2:n.1401G= | ||
ENST00000677462.1:n.2815G= | ||
ENST00000678975.1:n.2598G= | ||
ENST00000263774.8:c.382-41G= | ENSP00000263774.4:n.382-41G= | |
ENST00000524568.1:n.485-41G= | ||
ENST00000525378.5:n.279G= | ||
ENST00000533507.5:n.1276-41G= | ||
NM_004551.2:c.382-41G= | NP_004542.1:n.382-41G= | |
NM_004551.3:c.382-41G= MANE Select | NP_004542.1:n.382-41G= |