HGVS | Genome Assembly |
---|---|
NC_000003.12:g.28887369T= , CM000665.2:g.28887369T= | GRCh38 |
NC_000003.11:g.28928860T= , CM000665.1:g.28928860T= | GRCh37 |
NC_000003.10:g.28903864T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000635992.1:c.*408+22077T= | ENSP00000489994.1:n.*408+22077T= | |
ENST00000636582.1:n.238+22077T= | ||
ENST00000636680.2:c.282+22077T= | ENSP00000490271.2:n.282+22077T= | |
ENST00000636900.1:n.238+22077T= | ||
ENST00000637842.1:c.70-11115T= | ENSP00000489718.1:n.70-11115T= |