HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1213421_1213422insT , CM000667.2:g.1213421_1213422insT | GRCh38 |
NC_000005.9:g.1213536_1213537insT , CM000667.1:g.1213536_1213537insT | GRCh37 |
NC_000005.8:g.1266536_1266537insT | NCBI36 |
NG_008282.1:g.16827_16828insT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000304460.11:c.664-42_664-41insT MANE Select | ENSP00000305302.10:n.664-42_664-41insT | |
ENST00000304460.10:c.664-42_664-41insT | ENSP00000305302.10:n.664-42_664-41insT | |
ENST00000515652.5:c.572-42_572-41insT | ENSP00000425701.1:n.572-42_572-41insT | |
NM_001003841.2:c.664-42_664-41insT | NP_001003841.1:n.664-42_664-41insT | |
NM_001003841.3:c.664-42_664-41insT MANE Select | NP_001003841.1:n.664-42_664-41insT |