HGVS | Genome Assembly |
---|---|
NC_000005.10:g.96416057C= , CM000667.2:g.96416057C= | GRCh38 |
NC_000005.9:g.95751761C= , CM000667.1:g.95751761C= | GRCh37 |
NC_000005.8:g.95777517C= | NCBI36 |
NG_021161.1:g.22225G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000311106.8:c.685G= MANE Select | ENSP00000308024.2:p.Val229= | |
ENST00000311106.7:c.685G= | ENSP00000308024.2:p.Val229= | |
ENST00000508626.5:c.544G= | ENSP00000421600.1:p.Val182= | |
NM_000439.4:c.685G= | NP_000430.3:p.Val229= | |
NM_001177875.1:c.544G= | NP_001171346.1:p.Val182= | |
NR_130776.1:n.354+36405C= | ||
NM_000439.5:c.685G= MANE Select | NP_000430.3:p.Val229= | |
NM_001177875.2:c.544G= | NP_001171346.1:p.Val182= |