HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5226497T= , CM000673.2:g.5226497T= | GRCh38 |
NC_000011.9:g.5247727T= , CM000673.1:g.5247727T= | GRCh37 |
NC_000011.8:g.5204303T= | NCBI36 |
NG_000007.3:g.71119A= | |
NG_059281.1:g.5575A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647020.1:c.315+80A= | ENSP00000494175.1:n.315+80A= | |
ENST00000335295.4:c.315+80A= MANE Select | ENSP00000333994.3:n.315+80A= | |
ENST00000475226.1:n.247+80A= | ||
ENST00000485743.1:n.446A= | ||
ENST00000633227.1:c.*131+80A= | ENSP00000488004.1:n.*131+80A= | |
NM_000518.4:c.315+80A= | NP_000509.1:n.315+80A= | |
NM_000518.5:c.315+80A= MANE Select | NP_000509.1:n.315+80A= |