HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32634222_32634223insCT , CM000668.2:g.32634222_32634223insCT | GRCh38 |
NC_000006.11:g.32601999_32602000insCT , CM000668.1:g.32601999_32602000insCT | GRCh37 |
NC_000006.10:g.32709977_32709978insCT | NCBI36 |
NG_032876.1:g.1817_1818insCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000422863.1:c.-39+1313_-39+1314insCT | ENSP00000405797.1:n.-39+1313_-39+1314insCT |