HGVS | Genome Assembly |
---|---|
NC_000012.12:g.72011432del , CM000674.2:g.72011432del | GRCh38 |
NC_000012.11:g.72405212del , CM000674.1:g.72405212del | GRCh37 |
NC_000012.10:g.70691479del | NCBI36 |
NG_008279.1:g.77587del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000333850.4:c.1069-10967del MANE Select | ENSP00000329093.3:n.1069-10967del | |
ENST00000333850.3:c.1069-10967del | ENSP00000329093.3:n.1069-10967del | |
NM_173353.3:c.1069-10967del | NP_775489.2:n.1069-10967del | |
XM_011537899.1:c.475-10967del | XP_011536201.1:n.475-10967del | |
NM_173353.4:c.1069-10967del MANE Select | NP_775489.2:n.1069-10967del |