HGVS | Genome Assembly |
---|---|
NC_000011.10:g.124872926C>G , CM000673.2:g.124872926C>G | GRCh38 |
NC_000011.9:g.124742822C>G , CM000673.1:g.124742822C>G | GRCh37 |
NC_000011.8:g.124248032C>G | NCBI36 |
NG_016214.1:g.12518C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000397801.6:c.1373C>G MANE Select | ENSP00000380903.1:p.Ala458Gly | |
ENST00000397801.5:c.1373C>G | ENSP00000380903.1:p.Ala458Gly | |
ENST00000538940.5:c.1307C>G | ENSP00000441797.1:p.Ala436Gly | |
NM_022370.3:c.1373C>G | NP_071765.2:p.Ala458Gly | |
XM_011542953.1:c.2345C>G | XP_011541255.1:p.Ala782Gly | |
XM_017018122.1:c.1307C>G | XP_016873611.1:p.Ala436Gly | |
NM_022370.4:c.1373C>G MANE Select | NP_071765.2:p.Ala458Gly |