HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5250023C= , CM000673.2:g.5250023C= | GRCh38 |
NC_000011.9:g.5271253C= , CM000673.1:g.5271253C= | GRCh37 |
NC_000011.8:g.5227829C= | NCBI36 |
NG_000007.3:g.47593G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000642908.1:c.316-1536G= | ENSP00000495346.1:n.316-1536G= | |
ENST00000647543.1:c.379-1536G= | ENSP00000496470.1:n.379-1536G= | |
ENST00000620888.4:c.316-1536G= | ENSP00000479637.1:n.316-1536G= |