HGVS | Genome Assembly |
---|---|
NC_000001.11:g.109264411_109264412del , CM000663.2:g.109264411_109264412del | GRCh38 |
NC_000001.10:g.109807033_109807034del , CM000663.1:g.109807033_109807034del | GRCh37 |
NC_000001.9:g.109608556_109608557del | NCBI36 |
NG_052669.1:g.19707_19708del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271332.4:c.5290-43_5290-42del MANE Select | ENSP00000271332.3:n.5290-43_5290-42del | |
ENST00000271332.3:c.5290-43_5290-42del | ENSP00000271332.3:n.5290-43_5290-42del | |
NM_001408.2:c.5290-43_5290-42del | NP_001399.1:n.5290-43_5290-42del | |
XM_005270580.3:c.5290-43_5290-42del | XP_005270637.1:n.5290-43_5290-42del | |
NM_001408.3:c.5290-43_5290-42del MANE Select | NP_001399.1:n.5290-43_5290-42del |