HGVS | Genome Assembly |
---|---|
NC_000017.11:g.61590568_61590570del , CM000679.2:g.61590568_61590570del | GRCh38 |
NC_000017.10:g.59667929_59667931del , CM000679.1:g.59667929_59667931del | GRCh37 |
NC_000017.9:g.57022711_57022713del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000521764.3:c.613_615del MANE Select | ENSP00000427802.1:p.Asp205del | |
ENST00000521764.2:c.613_615del | ENSP00000427802.1:p.Asp205del | |
NM_199290.3:c.613_615del | NP_954984.1:p.Asp205del | |
NM_199290.4:c.613_615del MANE Select | NP_954984.1:p.Asp205del |