HGVS | Genome Assembly |
---|---|
NC_000002.12:g.197706499A>G , CM000664.2:g.197706499A>G | GRCh38 |
NC_000002.11:g.198571223A>G , CM000664.1:g.198571223A>G | GRCh37 |
NC_000002.10:g.198279468A>G | NCBI36 |
NG_034122.1:g.6196A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000282276.8:c.1094A>G MANE Select | ENSP00000282276.6:p.Tyr365Cys | |
ENST00000282276.7:c.1094A>G | ENSP00000282276.6:p.Tyr365Cys | |
NM_138395.3:c.1094A>G | NP_612404.1:p.Tyr365Cys | |
NM_138395.4:c.1094A>G MANE Select | NP_612404.1:p.Tyr365Cys |