HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1213341_1213393del , CM000667.2:g.1213341_1213393del | GRCh38 |
NC_000005.9:g.1213456_1213508del , CM000667.1:g.1213456_1213508del | GRCh37 |
NC_000005.8:g.1266456_1266508del | NCBI36 |
NG_008282.1:g.16747_16799del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304460.11:c.664-122_664-70del MANE Select | ENSP00000305302.10:n.664-122_664-70del | |
ENST00000304460.10:c.664-122_664-70del | ENSP00000305302.10:n.664-122_664-70del | |
ENST00000515652.5:c.572-122_572-70del | ENSP00000425701.1:n.572-122_572-70del | |
NM_001003841.2:c.664-122_664-70del | NP_001003841.1:n.664-122_664-70del | |
NM_001003841.3:c.664-122_664-70del MANE Select | NP_001003841.1:n.664-122_664-70del |