HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17381945del , CM000663.2:g.17381945del | GRCh38 |
NC_000001.10:g.17708440del , CM000663.1:g.17708440del | GRCh37 |
NC_000001.9:g.17581027del | NCBI36 |
NG_032943.1:g.14700del | |
NG_032943.2:g.14700del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000619609.1:c.554-22del MANE Select | ENSP00000483125.1:n.554-22del | |
NM_207421.4:c.554-22del MANE Select | NP_997304.3:n.554-22del |