HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42909375T>G , CM000679.2:g.42909375T>G | GRCh38 |
NC_000017.10:g.41061392T>G , CM000679.1:g.41061392T>G | GRCh37 |
NC_000017.9:g.38314918T>G | NCBI36 |
NG_011808.1:g.13578T>G , LRG_147:g.13578T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000253801.7:c.519T>G MANE Select | ENSP00000253801.1:p.Leu173= | |
ENST00000253801.6:c.519T>G | ENSP00000253801.1:p.Leu173= | |
ENST00000585489.1:c.447-1540T>G | ENSP00000466202.1:n.447-1540T>G | |
ENST00000592383.5:c.442T>G | ENSP00000465958.1:p.Cys148Gly | |
NM_000151.3:c.519T>G | NP_000142.2:p.Leu173= | |
NM_001270397.1:c.442T>G | NP_001257326.1:p.Cys148Gly | |
NM_000151.4:c.519T>G MANE Select | NP_000142.2:p.Leu173= | |
NM_001270397.2:c.442T>G | NP_001257326.1:p.Cys148Gly |