HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140333372_140333373insCCATAG , CM000667.2:g.140333372_140333373insCCATAG | GRCh38 |
NC_000005.9:g.139712957_139712958insCCATAG , CM000667.1:g.139712957_139712958insCCATAG | GRCh37 |
NC_000005.8:g.139693141_139693142insCCATAG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000230990.7:c.*926_*927insCTATGG MANE Select | ENSP00000230990.6:n.*926_*927insCTATGG | |
ENST00000230990.6:c.*926_*927insCTATGG | ENSP00000230990.6:n.*926_*927insCTATGG | |
NM_001945.2:c.*926_*927insCTATGG | NP_001936.1:n.*926_*927insCTATGG | |
NM_001945.3:c.*926_*927insCTATGG MANE Select | NP_001936.1:n.*926_*927insCTATGG |