HGVS | Genome Assembly |
---|---|
NC_000023.11:g.78113823C>G , CM000685.2:g.78113823C>G | GRCh38 |
NC_000023.10:g.77369320C>G , CM000685.1:g.77369320C>G | GRCh37 |
NC_000023.9:g.77255976C>G | NCBI36 |
NG_008862.1:g.14655C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373316.5:c.196C>G MANE Select | ENSP00000362413.4:p.Arg66Gly | |
ENST00000644362.1:c.112C>G | ENSP00000496140.1:p.Arg38Gly | |
ENST00000373316.4:c.196C>G | ENSP00000362413.4:p.Arg66Gly | |
ENST00000477335.5:n.332C>G | ||
ENST00000491291.1:n.188C>G | ||
NM_000291.3:c.196C>G | NP_000282.1:p.Arg66Gly | |
NM_000291.4:c.196C>G MANE Select | NP_000282.1:p.Arg66Gly |