HGVS | Genome Assembly |
---|---|
NC_000005.10:g.10286367C= , CM000667.2:g.10286367C= | GRCh38 |
NC_000005.9:g.10286479C= , CM000667.1:g.10286479C= | GRCh37 |
NC_000005.8:g.10339479C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296658.4:c.453G= MANE Select | ENSP00000296658.3:p.Gly151= | |
ENST00000296658.3:c.453G= | ENSP00000296658.3:p.Gly151= | |
ENST00000506821.1:n.707G= | ||
ENST00000510532.5:n.521G= | ||
ENST00000511963.5:n.561G= | ||
NM_138809.3:c.453G= | NP_620164.1:p.Gly151= | |
NM_138809.4:c.453G= MANE Select | NP_620164.1:p.Gly151= |