HGVS | Genome Assembly |
---|---|
NC_000011.10:g.6319215C= , CM000673.2:g.6319215C= | GRCh38 |
NC_000011.9:g.6340445C= , CM000673.1:g.6340445C= | GRCh37 |
NC_000011.8:g.6297021C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303927.4:c.734G= MANE Select | ENSP00000307292.3:p.Gly245= | |
ENST00000303927.3:c.734G= | ENSP00000307292.3:p.Gly245= | |
ENST00000524852.1:n.520G= | ||
ENST00000530979.1:c.830G= | ENSP00000432047.1:p.Gly277= | |
ENST00000532354.1:n.756G= | ||
NM_145040.2:c.734G= | NP_659477.2:p.Gly245= | |
XR_930997.1:n.720+995C= | ||
XR_242848.4:n.75C= | ||
NM_145040.3:c.734G= MANE Select | NP_659477.2:p.Gly245= |