HGVS | Genome Assembly |
---|---|
NC_000011.10:g.6868503C= , CM000673.2:g.6868503C= | GRCh38 |
NC_000011.9:g.6889734C= , CM000673.1:g.6889734C= | GRCh37 |
NC_000011.8:g.6846310C= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000641461.1:c.-132-1120C= (OR10A2) MANE Select | ENSP00000493131.1:n.-132-1120C= | |
XM_011520058.1:c.-436+29590G= (OR2AG2) | XP_011518360.1:n.-436+29590G= | |
XM_011520059.1:c.-436+29590G= (OR2AG2) | XP_011518361.1:n.-436+29590G= | |
XM_011520060.1:c.-436+29590G= (OR2AG2) | XP_011518362.1:n.-436+29590G= | |
XM_011520061.1:c.-436+55995G= (OR2AG2) | XP_011518363.1:n.-436+55995G= | |
NM_001004460.2:c.-132-1120C= (OR10A2) MANE Select | NP_001004460.1:n.-132-1120C= |