HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5253159A= , CM000673.2:g.5253159A= | GRCh38 |
NC_000011.9:g.5274389A= , CM000673.1:g.5274389A= | GRCh37 |
NC_000011.8:g.5230965A= | NCBI36 |
NG_000007.3:g.44457T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000642908.1:c.315+1133T= | ENSP00000495346.1:n.315+1133T= | |
ENST00000647543.1:c.378+184T= | ENSP00000496470.1:n.378+184T= | |
ENST00000620888.4:c.315+1133T= | ENSP00000479637.1:n.315+1133T= |