HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31519817A>G , CM000680.2:g.31519817A>G | GRCh38 |
NC_000018.9:g.29099780A>G , CM000680.1:g.29099780A>G | GRCh37 |
NC_000018.8:g.27353778A>G | NCBI36 |
NG_007072.3:g.26576A>G , LRG_397:g.26576A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682241.2:c.96A>G | ENSP00000507600.2:p.Arg32= | |
ENST00000683654.1:c.96A>G | ENSP00000506971.1:p.Arg32= | |
ENST00000261590.13:c.96A>G MANE Select | ENSP00000261590.8:p.Arg32= | |
ENST00000261590.12:c.96A>G | ENSP00000261590.8:p.Arg32= | |
ENST00000585206.1:c.96A>G | ENSP00000462503.1:p.Arg32= | |
NM_001943.3:c.96A>G , LRG_397t1:c.96A>G | NP_001934.2:p.Arg32= | |
NM_001943.4:c.96A>G | NP_001934.2:p.Arg32= | |
XM_024451095.1:c.-439A>G | XP_024306863.1:n.-439A>G | |
NM_001943.5:c.96A>G MANE Select | NP_001934.2:p.Arg32= |