HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55156206G>C , CM000681.2:g.55156206G>C | GRCh38 |
NC_000019.9:g.55667574G>C , CM000681.1:g.55667574G>C | GRCh37 |
NC_000019.8:g.60359386G>C | NCBI36 |
NG_007866.2:g.6527C>G , LRG_432:g.6527C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.277C>G MANE Select | ENSP00000341838.5:p.Leu93Val | |
ENST00000665070.1:c.277C>G | ENSP00000499482.1:p.Leu93Val | |
ENST00000344887.9:c.277C>G | ENSP00000341838.5:p.Leu93Val | |
ENST00000585806.5:n.276C>G | ||
ENST00000586669.5:n.285C>G | ||
ENST00000587176.5:n.461C>G | ||
ENST00000587871.1:c.896C>G | ||
ENST00000588882.1:c.202C>G | ENSP00000466729.1:p.Leu68Val | |
ENST00000590463.1:n.449C>G | ||
NM_000363.4:c.277C>G , LRG_432t1:c.277C>G | NP_000354.4:p.Leu93Val | |
NM_000363.5:c.277C>G MANE Select | NP_000354.4:p.Leu93Val |