HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1213853del , CM000667.2:g.1213853del | GRCh38 |
NC_000005.9:g.1213968del , CM000667.1:g.1213968del | GRCh37 |
NC_000005.8:g.1266968del | NCBI36 |
NG_008282.1:g.17259del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304460.11:c.775-100del MANE Select | ENSP00000305302.10:n.775-100del | |
ENST00000304460.10:c.775-100del | ENSP00000305302.10:n.775-100del | |
ENST00000515652.5:c.683-100del | ENSP00000425701.1:n.683-100del | |
NM_001003841.2:c.775-100del | NP_001003841.1:n.775-100del | |
NM_001003841.3:c.775-100del MANE Select | NP_001003841.1:n.775-100del |