HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160127659A>G , CM000663.2:g.160127659A>G | GRCh38 |
NC_000001.10:g.160097449A>G , CM000663.1:g.160097449A>G | GRCh37 |
NC_000001.9:g.158364073A>G | NCBI36 |
NG_008014.1:g.16902A>G , LRG_6:g.16902A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361216.8:c.856A>G MANE Select | ENSP00000354490.3:p.Ile286Val | |
ENST00000361216.7:c.856A>G | ENSP00000354490.3:p.Ile286Val | |
ENST00000392233.7:c.856A>G | ENSP00000376066.3:p.Ile286Val | |
ENST00000472488.5:n.959A>G | ||
NM_000702.3:c.856A>G | NP_000693.1:p.Ile286Val | |
NM_000702.4:c.856A>G MANE Select | NP_000693.1:p.Ile286Val |