HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55156216G>C , CM000681.2:g.55156216G>C | GRCh38 |
NC_000019.9:g.55667584G>C , CM000681.1:g.55667584G>C | GRCh37 |
NC_000019.8:g.60359396G>C | NCBI36 |
NG_007866.2:g.6517C>G , LRG_432:g.6517C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.267C>G MANE Select | ENSP00000341838.5:p.Gly89= | |
ENST00000665070.1:c.267C>G | ENSP00000499482.1:p.Gly89= | |
ENST00000344887.9:c.267C>G | ENSP00000341838.5:p.Gly89= | |
ENST00000585806.5:n.266C>G | ||
ENST00000586669.5:n.275C>G | ||
ENST00000587176.5:n.451C>G | ||
ENST00000587871.1:c.886C>G | ||
ENST00000588882.1:c.192C>G | ENSP00000466729.1:p.Gly64= | |
ENST00000590463.1:n.439C>G | ||
NM_000363.4:c.267C>G , LRG_432t1:c.267C>G | NP_000354.4:p.Gly89= | |
NM_000363.5:c.267C>G MANE Select | NP_000354.4:p.Gly89= |