HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659195T>G , CM000685.2:g.136659195T>G | GRCh38 |
NC_000023.10:g.135741354T>G , CM000685.1:g.135741354T>G | GRCh37 |
NC_000023.9:g.135569020T>G | NCBI36 |
NG_007280.1:g.16019T>G , LRG_141:g.16019T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*184T>G | ENSP00000512122.1:n.*184T>G | |
ENST00000695725.1:c.*121T>G | ENSP00000512123.1:n.*121T>G | |
ENST00000695726.1:n.2534T>G | ||
ENST00000695729.1:n.3369T>G | ||
ENST00000370629.7:c.566T>G MANE Select | ENSP00000359663.2:p.Phe189Cys | |
ENST00000370628.2:c.503T>G | ENSP00000359662.2:p.Phe168Cys | |
ENST00000370629.6:c.566T>G | ENSP00000359663.2:p.Phe189Cys | |
NM_000074.2:c.566T>G , LRG_141t1:c.566T>G | NP_000065.1:p.Phe189Cys | |
NM_000074.3:c.566T>G MANE Select | NP_000065.1:p.Phe189Cys |