HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1213377_1213379del , CM000667.2:g.1213377_1213379del | GRCh38 |
NC_000005.9:g.1213492_1213494del , CM000667.1:g.1213492_1213494del | GRCh37 |
NC_000005.8:g.1266492_1266494del | NCBI36 |
NG_008282.1:g.16783_16785del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304460.11:c.664-86_664-84del MANE Select | ENSP00000305302.10:n.664-86_664-84del | |
ENST00000304460.10:c.664-86_664-84del | ENSP00000305302.10:n.664-86_664-84del | |
ENST00000515652.5:c.572-86_572-84del | ENSP00000425701.1:n.572-86_572-84del | |
NM_001003841.2:c.664-86_664-84del | NP_001003841.1:n.664-86_664-84del | |
NM_001003841.3:c.664-86_664-84del MANE Select | NP_001003841.1:n.664-86_664-84del |