HGVS | Genome Assembly |
---|---|
NC_000001.11:g.209796495T>C , CM000663.2:g.209796495T>C | GRCh38 |
NC_000001.10:g.209969840T>C , CM000663.1:g.209969840T>C | GRCh37 |
NC_000001.9:g.208036463T>C | NCBI36 |
NG_007081.2:g.14640A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696133.1:c.232A>G | ENSP00000512426.1:p.Lys78Glu | |
ENST00000696134.1:c.232A>G | ENSP00000512427.1:p.Lys78Glu | |
ENST00000367021.8:c.232A>G MANE Select | ENSP00000355988.3:p.Lys78Glu | |
ENST00000643798.1:c.232A>G | ENSP00000496669.1:p.Lys78Glu | |
ENST00000367021.7:c.232A>G | ENSP00000355988.3:p.Lys78Glu | |
ENST00000456314.1:c.232A>G | ENSP00000403855.1:p.Lys78Glu | |
ENST00000542854.5:c.-54A>G | ENSP00000440532.1:n.-54A>G | |
NM_001206696.1:c.-54A>G | NP_001193625.1:n.-54A>G | |
NM_006147.3:c.232A>G | NP_006138.1:p.Lys78Glu | |
NM_006147.4:c.232A>G MANE Select | NP_006138.1:p.Lys78Glu | |
NM_001206696.2:c.-54A>G | NP_001193625.1:n.-54A>G |