HGVS | Genome Assembly |
---|---|
NC_000005.10:g.96416096T>C , CM000667.2:g.96416096T>C | GRCh38 |
NC_000005.9:g.95751800T>C , CM000667.1:g.95751800T>C | GRCh37 |
NC_000005.8:g.95777556T>C | NCBI36 |
NG_021161.1:g.22186A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000311106.8:c.646A>G MANE Select | ENSP00000308024.2:p.Ile216Val | |
ENST00000311106.7:c.646A>G | ENSP00000308024.2:p.Ile216Val | |
ENST00000508626.5:c.505A>G | ENSP00000421600.1:p.Ile169Val | |
NM_000439.4:c.646A>G | NP_000430.3:p.Ile216Val | |
NM_001177875.1:c.505A>G | NP_001171346.1:p.Ile169Val | |
NR_130776.1:n.354+36444T>C | ||
NM_000439.5:c.646A>G MANE Select | NP_000430.3:p.Ile216Val | |
NM_001177875.2:c.505A>G | NP_001171346.1:p.Ile169Val |