HGVS | Genome Assembly |
---|---|
NC_000001.11:g.11965567C>G , CM000663.2:g.11965567C>G | GRCh38 |
NC_000001.10:g.12025624C>G , CM000663.1:g.12025624C>G | GRCh37 |
NC_000001.9:g.11948211C>G | NCBI36 |
NG_008159.1:g.35879C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000196061.5:c.1558C>G MANE Select | ENSP00000196061.4:p.Leu520Val | |
ENST00000196061.4:c.1558C>G | ENSP00000196061.4:p.Leu520Val | |
ENST00000470133.1:n.172C>G | ||
ENST00000491536.5:n.186C>G | ||
NM_000302.3:c.1558C>G | NP_000293.2:p.Leu520Val | |
NM_001316320.1:c.1699C>G | NP_001303249.1:p.Leu567Val | |
XM_011541594.1:c.1639C>G | XP_011539896.1:p.Leu547Val | |
XM_024447707.1:c.892C>G | XP_024303475.1:p.Leu298Val | |
NM_000302.4:c.1558C>G MANE Select | NP_000293.2:p.Leu520Val | |
NM_001316320.2:c.1699C>G | NP_001303249.1:p.Leu567Val |