HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17395782del , CM000663.2:g.17395782del | GRCh38 |
NC_000001.10:g.17722278del , CM000663.1:g.17722278del | GRCh37 |
NC_000001.9:g.17594865del | NCBI36 |
NG_032943.1:g.28537del | |
NG_032943.2:g.28537del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000619609.1:c.1618+119del MANE Select | ENSP00000483125.1:n.1618+119del | |
NM_207421.4:c.1618+119del MANE Select | NP_997304.3:n.1618+119del |