HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4631245_4631247dup , CM000679.2:g.4631245_4631247dup | GRCh38 |
NC_000017.10:g.4534540_4534542dup , CM000679.1:g.4534540_4534542dup | GRCh37 |
NC_000017.9:g.4481289_4481291dup | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293761.8:c.*357_*359dup MANE Select | ENSP00000293761.3:n.*357_*359dup | |
ENST00000293761.7:c.*357_*359dup | ENSP00000293761.3:n.*357_*359dup | |
ENST00000570836.5:c.*357_*359dup | ENSP00000458832.1:n.*357_*359dup | |
NM_001140.3:c.*357_*359dup | NP_001131.3:n.*357_*359dup | |
NM_001140.4:c.*357_*359dup | NP_001131.3:n.*357_*359dup | |
NM_001140.5:c.*357_*359dup MANE Select | NP_001131.3:n.*357_*359dup |