HGVS | Genome Assembly |
---|---|
NC_000011.10:g.8101855T>A , CM000673.2:g.8101855T>A | GRCh38 |
NC_000011.9:g.8123402T>A , CM000673.1:g.8123402T>A | GRCh37 |
NC_000011.8:g.8079978T>A | NCBI36 |
NG_029912.1:g.68223T>A | |
NG_030416.2:g.72189A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299506.3:c.*236T>A (TUB) MANE Select | ENSP00000299506.3:n.*236T>A | |
ENST00000299506.2:c.*236T>A (TUB) | ENSP00000299506.2:n.*236T>A | |
ENST00000305253.8:c.*236T>A (TUB) | ENSP00000305426.4:n.*236T>A | |
NM_003320.4:c.*236T>A (TUB) | NP_003311.2:n.*236T>A | |
NM_177972.2:c.*236T>A (TUB) | NP_813977.1:n.*236T>A | |
XM_005253109.2:c.*236T>A (TUB) | XP_005253166.1:n.*236T>A | |
XM_011520344.1:c.*236T>A (TUB) | XP_011518646.1:n.*236T>A | |
XR_428851.2:n.1484-7696A>T (RIC3) | ||
XR_930896.1:n.1546+5480A>T (RIC3) | ||
XR_930900.1:n.1547-4133A>T (RIC3) | ||
NR_144485.1:n.1519+5480A>T (RIC3) | ||
XM_005253109.3:c.*236T>A (TUB) | XP_005253166.1:n.*236T>A | |
XM_011520344.2:c.*236T>A (TUB) | XP_011518646.1:n.*236T>A | |
XR_001747957.2:n.1335-7696A>T (RIC3) | ||
XR_428851.4:n.1422-7696A>T (RIC3) | ||
XR_930896.3:n.1484+5480A>T (RIC3) | ||
XR_930900.3:n.1485-4133A>T (RIC3) | ||
NM_177972.3:c.*236T>A (TUB) MANE Select | NP_813977.1:n.*236T>A | |
NR_144485.2:n.1450+5480A>T (RIC3) | ||
NM_003320.5:c.*236T>A (TUB) | NP_003311.2:n.*236T>A |