HGVS | Genome Assembly |
---|---|
NC_000003.12:g.29167543T>G , CM000665.2:g.29167543T>G | GRCh38 |
NC_000003.11:g.29209034T>G , CM000665.1:g.29209034T>G | GRCh37 |
NC_000003.10:g.29184038T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000635992.1:c.*409-15413T>G | ENSP00000489994.1:n.*409-15413T>G | |
ENST00000636582.1:n.353-15413T>G | ||
ENST00000636680.2:c.283-15413T>G | ENSP00000490271.2:n.283-15413T>G | |
ENST00000636900.1:n.239-15413T>G | ||
ENST00000637842.1:c.149-15413T>G | ENSP00000489718.1:n.149-15413T>G |