HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140333319del , CM000667.2:g.140333319del | GRCh38 |
NC_000005.9:g.139712904del , CM000667.1:g.139712904del | GRCh37 |
NC_000005.8:g.139693088del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000230990.7:c.*980del MANE Select | ENSP00000230990.6:n.*980del | |
ENST00000230990.6:c.*980del | ENSP00000230990.6:n.*980del | |
NM_001945.2:c.*980del | NP_001936.1:n.*980del | |
NM_001945.3:c.*980del MANE Select | NP_001936.1:n.*980del |