HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47582279A= , CM000673.2:g.47582279A= | GRCh38 |
NC_000011.9:g.47603831A= , CM000673.1:g.47603831A= | GRCh37 |
NC_000011.8:g.47560407A= | NCBI36 |
NG_011946.1:g.8270A= | |
NG_011946.2:g.8270A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000263774.9:c.507+66A= MANE Select | ENSP00000263774.4:n.507+66A= | |
ENST00000531351.2:n.1633A= | ||
ENST00000677462.1:n.2981+66A= | ||
ENST00000678975.1:n.2764+66A= | ||
ENST00000263774.8:c.507+66A= | ENSP00000263774.4:n.507+66A= | |
ENST00000524568.1:n.610+66A= | ||
ENST00000525212.1:n.162+66A= | ||
ENST00000525378.5:n.445+66A= | ||
ENST00000527178.1:n.38A= | ||
ENST00000533507.5:n.1401+66A= | ||
NM_004551.2:c.507+66A= | NP_004542.1:n.507+66A= | |
NM_004551.3:c.507+66A= MANE Select | NP_004542.1:n.507+66A= |