HGVS | Genome Assembly |
---|---|
NC_000019.10:g.10115543G>C , CM000681.2:g.10115543G>C | GRCh38 |
NC_000019.9:g.10226219G>C , CM000681.1:g.10226219G>C | GRCh37 |
NC_000019.8:g.10087219G>C | NCBI36 |
NG_047007.1:g.9023G>C | |
NG_051197.1:g.9382C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000253108.9:c.883C>G MANE Select | ENSP00000253108.3:p.Arg295Gly | |
ENST00000253108.8:c.883C>G | ENSP00000253108.3:p.Arg295Gly | |
ENST00000589454.5:c.859C>G | ENSP00000466860.1:p.Arg287Gly | |
ENST00000590158.1:n.902C>G | ||
ENST00000593054.5:c.277C>G | ENSP00000467187.1:p.Arg93Gly | |
NM_003755.3:c.883C>G | NP_003746.2:p.Arg295Gly | |
NM_003755.4:c.883C>G | NP_003746.2:p.Arg295Gly | |
NM_003755.5:c.883C>G MANE Select | NP_003746.2:p.Arg295Gly |