HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1213368_1213369insGC , CM000667.2:g.1213368_1213369insGC | GRCh38 |
NC_000005.9:g.1213483_1213484insGC , CM000667.1:g.1213483_1213484insGC | GRCh37 |
NC_000005.8:g.1266483_1266484insGC | NCBI36 |
NG_008282.1:g.16774_16775insGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304460.11:c.664-95_664-94insGC MANE Select | ENSP00000305302.10:n.664-95_664-94insGC | |
ENST00000304460.10:c.664-95_664-94insGC | ENSP00000305302.10:n.664-95_664-94insGC | |
ENST00000515652.5:c.572-95_572-94insGC | ENSP00000425701.1:n.572-95_572-94insGC | |
NM_001003841.2:c.664-95_664-94insGC | NP_001003841.1:n.664-95_664-94insGC | |
NM_001003841.3:c.664-95_664-94insGC MANE Select | NP_001003841.1:n.664-95_664-94insGC |