HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659213T>G , CM000685.2:g.136659213T>G | GRCh38 |
NC_000023.10:g.135741372T>G , CM000685.1:g.135741372T>G | GRCh37 |
NC_000023.9:g.135569038T>G | NCBI36 |
NG_007280.1:g.16037T>G , LRG_141:g.16037T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*202T>G | ENSP00000512122.1:n.*202T>G | |
ENST00000695725.1:c.*139T>G | ENSP00000512123.1:n.*139T>G | |
ENST00000695726.1:n.2552T>G | ||
ENST00000695729.1:n.3387T>G | ||
ENST00000370629.7:c.584T>G MANE Select | ENSP00000359663.2:p.Leu195Arg | |
ENST00000370628.2:c.521T>G | ENSP00000359662.2:p.Leu174Arg | |
ENST00000370629.6:c.584T>G | ENSP00000359663.2:p.Leu195Arg | |
NM_000074.2:c.584T>G , LRG_141t1:c.584T>G | NP_000065.1:p.Leu195Arg | |
NM_000074.3:c.584T>G MANE Select | NP_000065.1:p.Leu195Arg |