HGVS | Genome Assembly |
---|---|
NC_000001.11:g.214622139A>G , CM000663.2:g.214622139A>G | GRCh38 |
NC_000001.10:g.214795482A>G , CM000663.1:g.214795482A>G | GRCh37 |
NC_000001.9:g.212862105A>G | NCBI36 |
NG_046787.1:g.23961A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706764.1:n.1104A>G | ||
ENST00000706765.1:c.926A>G | ENSP00000516538.1:p.Lys309Arg | |
ENST00000366955.8:c.926A>G MANE Select | ENSP00000355922.3:p.Lys309Arg | |
ENST00000366955.7:c.926A>G | ENSP00000355922.3:p.Lys309Arg | |
NM_016343.3:c.926A>G | NP_057427.3:p.Lys309Arg | |
XM_011509082.1:c.926A>G | XP_011507384.1:p.Lys309Arg | |
XM_011509082.3:c.926A>G | XP_011507384.1:p.Lys309Arg | |
XM_017000086.2:c.926A>G | XP_016855575.1:p.Lys309Arg | |
NM_016343.4:c.926A>G MANE Select | NP_057427.3:p.Lys309Arg |