HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17393951_17393952insT , CM000663.2:g.17393951_17393952insT | GRCh38 |
NC_000001.10:g.17720447_17720448insT , CM000663.1:g.17720447_17720448insT | GRCh37 |
NC_000001.9:g.17593034_17593035insT | NCBI36 |
NG_032943.1:g.26706_26707insT | |
NG_032943.2:g.26706_26707insT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000619609.1:c.1075-24_1075-23insT MANE Select | ENSP00000483125.1:n.1075-24_1075-23insT | |
NM_207421.4:c.1075-24_1075-23insT MANE Select | NP_997304.3:n.1075-24_1075-23insT |