HGVS | Genome Assembly |
---|---|
NC_000005.10:g.175441486G= , CM000667.2:g.175441486G= | GRCh38 |
NC_000005.9:g.174868489G= , CM000667.1:g.174868489G= | GRCh37 |
NC_000005.8:g.174801095G= | NCBI36 |
NG_011802.1:g.7675C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000393752.3:c.*273C= MANE Select | ENSP00000377353.1:n.*273C= | |
ENST00000393752.2:c.*273C= | ENSP00000377353.1:n.*273C= | |
NM_000794.3:c.*273C= | NP_000785.1:n.*273C= | |
NM_000794.4:c.*273C= | NP_000785.1:n.*273C= | |
NM_000794.5:c.*273C= MANE Select | NP_000785.1:n.*273C= |