HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1213401_1213402delinsGC , CM000667.2:g.1213401_1213402delinsGC | GRCh38 |
NC_000005.9:g.1213516_1213517delinsGC , CM000667.1:g.1213516_1213517delinsGC | GRCh37 |
NC_000005.8:g.1266516_1266517delinsGC | NCBI36 |
NG_008282.1:g.16807_16808delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304460.11:c.664-62_664-61delinsGC MANE Select | ENSP00000305302.10:n.664-62_664-61delinsGC | |
ENST00000304460.10:c.664-62_664-61delinsGC | ENSP00000305302.10:n.664-62_664-61delinsGC | |
ENST00000515652.5:c.572-62_572-61delinsGC | ENSP00000425701.1:n.572-62_572-61delinsGC | |
NM_001003841.2:c.664-62_664-61delinsGC | NP_001003841.1:n.664-62_664-61delinsGC | |
NM_001003841.3:c.664-62_664-61delinsGC MANE Select | NP_001003841.1:n.664-62_664-61delinsGC |