HGVS | Genome Assembly |
---|---|
NC_000011.10:g.1075756A>G , CM000673.2:g.1075756A>G | GRCh38 |
NC_000011.9:g.1075756A>G , CM000673.1:g.1075756A>G | GRCh37 |
NC_000011.8:g.1065756A>G | NCBI36 |
NG_051929.1:g.5882A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361558.7:n.209A>G | ||
ENST00000675028.1:c.182A>G | ENSP00000502432.1:p.Tyr61Cys | |
NM_002457.3:c.182A>G | NP_002448.3:p.Tyr61Cys | |
NM_002457.4:c.182A>G | NP_002448.4:p.Tyr61Cys |