HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140333041_140333043del , CM000667.2:g.140333041_140333043del | GRCh38 |
NC_000005.9:g.139712626_139712628del , CM000667.1:g.139712626_139712628del | GRCh37 |
NC_000005.8:g.139692810_139692812del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000230990.7:c.*1256_*1258del MANE Select | ENSP00000230990.6:n.*1256_*1258del | |
ENST00000230990.6:c.*1256_*1258del | ENSP00000230990.6:n.*1256_*1258del | |
NM_001945.2:c.*1256_*1258del | NP_001936.1:n.*1256_*1258del | |
NM_001945.3:c.*1256_*1258del MANE Select | NP_001936.1:n.*1256_*1258del |