HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5253174A= , CM000673.2:g.5253174A= | GRCh38 |
NC_000011.9:g.5274404A= , CM000673.1:g.5274404A= | GRCh37 |
NC_000011.8:g.5230980A= | NCBI36 |
NG_000007.3:g.44442T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000642908.1:c.315+1118T= | ENSP00000495346.1:n.315+1118T= | |
ENST00000647543.1:c.378+169T= | ENSP00000496470.1:n.378+169T= | |
ENST00000620888.4:c.315+1118T= | ENSP00000479637.1:n.315+1118T= |