HGVS | Genome Assembly |
---|---|
NC_000003.12:g.164996797_164996800del , CM000665.2:g.164996797_164996800del | GRCh38 |
NC_000003.11:g.164714585_164714588del , CM000665.1:g.164714585_164714588del | GRCh37 |
NC_000003.10:g.166197279_166197282del | NCBI36 |
NG_017043.1:g.86696_86699del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264382.8:c.4541-28_4541-25del MANE Select | ENSP00000264382.3:n.4541-28_4541-25del | |
ENST00000264382.7:c.4541-28_4541-25del | ENSP00000264382.3:n.4541-28_4541-25del | |
NM_001041.3:c.4541-28_4541-25del | NP_001032.2:n.4541-28_4541-25del | |
XM_011513078.1:c.4442-28_4442-25del | XP_011511380.1:n.4442-28_4442-25del | |
XM_011513078.2:c.4442-28_4442-25del | XP_011511380.1:n.4442-28_4442-25del | |
NM_001041.4:c.4541-28_4541-25del MANE Select | NP_001032.2:n.4541-28_4541-25del |