Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6868417C= , CM000673.2:g.6868417C= | GRCh38 |
| NC_000011.9:g.6889648C= , CM000673.1:g.6889648C= | GRCh37 |
| NC_000011.8:g.6846224C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641461.1:c.-132-1206C= (OR10A2) MANE Select | ENSP00000493131.1:n.-132-1206C= | |
| XM_011520058.1:c.-436+29676G= (OR2AG2) | XP_011518360.1:n.-436+29676G= | |
| XM_011520059.1:c.-436+29676G= (OR2AG2) | XP_011518361.1:n.-436+29676G= | |
| XM_011520060.1:c.-436+29676G= (OR2AG2) | XP_011518362.1:n.-436+29676G= | |
| XM_011520061.1:c.-436+56081G= (OR2AG2) | XP_011518363.1:n.-436+56081G= | |
| NM_001004460.2:c.-132-1206C= (OR10A2) MANE Select | NP_001004460.1:n.-132-1206C= |