HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1212962_1212974del , CM000667.2:g.1212962_1212974del | GRCh38 |
NC_000005.9:g.1213077_1213089del , CM000667.1:g.1213077_1213089del | GRCh37 |
NC_000005.8:g.1266077_1266089del | NCBI36 |
NG_008282.1:g.16368_16380del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304460.11:c.663+478_664-489del MANE Select | ENSP00000305302.10:n.663+478_664-489del | |
ENST00000304460.10:c.663+478_664-489del | ENSP00000305302.10:n.663+478_664-489del | |
ENST00000515652.5:c.571+478_572-489del | ENSP00000425701.1:n.571+478_572-489del | |
NM_001003841.2:c.663+478_664-489del | NP_001003841.1:n.663+478_664-489del | |
NM_001003841.3:c.663+478_664-489del MANE Select | NP_001003841.1:n.663+478_664-489del |