HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171652050T>C , CM000663.2:g.171652050T>C | GRCh38 |
NC_000001.10:g.171621190T>C , CM000663.1:g.171621190T>C | GRCh37 |
NC_000001.9:g.169887813T>C | NCBI36 |
NG_008859.1:g.5584A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.562A>G MANE Select | ENSP00000037502.5:p.Thr188Ala | |
ENST00000638471.1:c.130+432A>G | ENSP00000491206.1:n.130+432A>G | |
ENST00000037502.10:c.562A>G | ENSP00000037502.5:p.Thr188Ala | |
ENST00000614688.1:c.562A>G | ENSP00000478680.1:p.Thr188Ala | |
NM_000261.1:c.562A>G | NP_000252.1:p.Thr188Ala | |
NM_000261.2:c.562A>G MANE Select | NP_000252.1:p.Thr188Ala |