HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1213419_1213420delinsGC , CM000667.2:g.1213419_1213420delinsGC | GRCh38 |
NC_000005.9:g.1213534_1213535delinsGC , CM000667.1:g.1213534_1213535delinsGC | GRCh37 |
NC_000005.8:g.1266534_1266535delinsGC | NCBI36 |
NG_008282.1:g.16825_16826delinsGC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000304460.11:c.664-44_664-43delinsGC MANE Select | ENSP00000305302.10:n.664-44_664-43delinsG... | |
ENST00000304460.10:c.664-44_664-43delinsGC | ENSP00000305302.10:n.664-44_664-43delinsG... | |
ENST00000515652.5:c.572-44_572-43delinsGC | ENSP00000425701.1:n.572-44_572-43delinsGC... | |
NM_001003841.2:c.664-44_664-43delinsGC | NP_001003841.1:n.664-44_664-43delinsGC | |
NM_001003841.3:c.664-44_664-43delinsGC MANE Select | NP_001003841.1:n.664-44_664-43delinsGC |