HGVS | Genome Assembly |
---|---|
NC_000001.11:g.109263990del , CM000663.2:g.109263990del | GRCh38 |
NC_000001.10:g.109806612del , CM000663.1:g.109806612del | GRCh37 |
NC_000001.9:g.109608135del | NCBI36 |
NG_052669.1:g.19286del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271332.4:c.5002-88del MANE Select | ENSP00000271332.3:n.5002-88del | |
ENST00000271332.3:c.5002-88del | ENSP00000271332.3:n.5002-88del | |
NM_001408.2:c.5002-88del | NP_001399.1:n.5002-88del | |
XM_005270580.3:c.5002-88del | XP_005270637.1:n.5002-88del | |
NM_001408.3:c.5002-88del MANE Select | NP_001399.1:n.5002-88del |