HGVS | Genome Assembly |
---|---|
NC_000021.9:g.46001284C>G , CM000683.2:g.46001284C>G | GRCh38 |
NC_000021.8:g.47421198C>G , CM000683.1:g.47421198C>G | GRCh37 |
NC_000021.7:g.46245626C>G | NCBI36 |
NG_008674.1:g.24536C>G , LRG_475:g.24536C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000463060.6:n.253C>G | ||
ENST00000361866.8:c.1854C>G MANE Select | ENSP00000355180.3:p.Phe618Leu | |
ENST00000361866.7:c.1854C>G | ENSP00000355180.3:p.Phe618Leu | |
ENST00000463060.5:n.253C>G | ||
ENST00000498614.5:n.88C>G | ||
ENST00000612273.1:c.1848C>G | ENSP00000483630.1:p.Phe616Leu | |
NM_001848.2:c.1854C>G , LRG_475t1:c.1854C>G | NP_001839.2:p.Phe618Leu | |
NM_001848.3:c.1854C>G MANE Select | NP_001839.2:p.Phe618Leu |