HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94418538C>G , CM000663.2:g.94418538C>G | GRCh38 |
NC_000001.10:g.94884094C>G , CM000663.1:g.94884094C>G | GRCh37 |
NC_000001.9:g.94656682C>G | NCBI36 |
NG_008865.1:g.5162C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370214.9:c.60C>G MANE Select | ENSP00000359233.4:p.Phe20Leu | |
ENST00000647998.2:c.60C>G | ENSP00000497921.2:p.Phe20Leu | |
ENST00000315713.5:c.60C>G | ENSP00000326880.5:p.Phe20Leu | |
ENST00000370214.8:c.60C>G | ENSP00000359233.4:p.Phe20Leu | |
NM_001122674.1:c.60C>G | NP_001116146.1:p.Phe20Leu | |
NM_002858.3:c.60C>G | NP_002849.1:p.Phe20Leu | |
XM_006710802.2:c.60C>G | XP_006710865.2:p.Phe20Leu | |
NM_002858.4:c.60C>G MANE Select | NP_002849.1:p.Phe20Leu | |
NM_001122674.2:c.60C>G | NP_001116146.1:p.Phe20Leu |