HGVS | Genome Assembly |
---|---|
NC_000011.10:g.124872516A>G , CM000673.2:g.124872516A>G | GRCh38 |
NC_000011.9:g.124742412A>G , CM000673.1:g.124742412A>G | GRCh37 |
NC_000011.8:g.124247622A>G | NCBI36 |
NG_016214.1:g.12108A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000397801.6:c.1294A>G MANE Select | ENSP00000380903.1:p.Ser432Gly | |
ENST00000397801.5:c.1294A>G | ENSP00000380903.1:p.Ser432Gly | |
ENST00000538940.5:c.1228A>G | ENSP00000441797.1:p.Ser410Gly | |
NM_022370.3:c.1294A>G | NP_071765.2:p.Ser432Gly | |
XM_011542953.1:c.2266A>G | XP_011541255.1:p.Ser756Gly | |
XM_017018122.1:c.1228A>G | XP_016873611.1:p.Ser410Gly | |
NM_022370.4:c.1294A>G MANE Select | NP_071765.2:p.Ser432Gly |