HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42911118A>G , CM000679.2:g.42911118A>G | GRCh38 |
NC_000017.10:g.41063135A>G , CM000679.1:g.41063135A>G | GRCh37 |
NC_000017.9:g.38316661A>G | NCBI36 |
NG_011808.1:g.15321A>G , LRG_147:g.15321A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000253801.7:c.766A>G MANE Select | ENSP00000253801.1:p.Thr256Ala | |
ENST00000253801.6:c.766A>G | ENSP00000253801.1:p.Thr256Ala | |
ENST00000585489.1:c.*158A>G | ENSP00000466202.1:n.*158A>G | |
ENST00000592383.5:c.*158A>G | ENSP00000465958.1:n.*158A>G | |
NM_000151.3:c.766A>G | NP_000142.2:p.Thr256Ala | |
NM_001270397.1:c.*158A>G | NP_001257326.1:n.*158A>G | |
NM_000151.4:c.766A>G MANE Select | NP_000142.2:p.Thr256Ala | |
NM_001270397.2:c.*158A>G | NP_001257326.1:n.*158A>G |