HGVS | Genome Assembly |
---|---|
NC_000011.10:g.6319462C>G , CM000673.2:g.6319462C>G | GRCh38 |
NC_000011.9:g.6340692C>G , CM000673.1:g.6340692C>G | GRCh37 |
NC_000011.8:g.6297268C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303927.4:c.487G>C MANE Select | ENSP00000307292.3:p.Gly163Arg | |
ENST00000303927.3:c.487G>C | ENSP00000307292.3:p.Gly163Arg | |
ENST00000524852.1:n.273G>C | ||
ENST00000530979.1:c.583G>C | ENSP00000432047.1:p.Gly195Arg | |
ENST00000532354.1:n.509G>C | ||
NM_145040.2:c.487G>C | NP_659477.2:p.Gly163Arg | |
XR_930997.1:n.720+1242C>G | ||
XR_001748106.1:n.73C>G | ||
XR_242848.4:n.322C>G | ||
NM_145040.3:c.487G>C MANE Select | NP_659477.2:p.Gly163Arg |