Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6845852A>G , CM000673.2:g.6845852A>G | GRCh38 |
| NC_000011.9:g.6867083A>G , CM000673.1:g.6867083A>G | GRCh37 |
| NC_000011.8:g.6823659A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_178168.1:c.170A>G (OR10A5) MANE Select | NP_835462.1:p.His57Arg |
| ENST00000299454.5:c.170A>G (OR10A5) MANE Select | ENSP00000299454.4:p.His57Arg |
| ENST00000299454.4:c.170A>G (OR10A5) | ENSP00000299454.4:p.His57Arg |
| XM_011520058.1:c.-436+52241T>C (OR2AG2) | XP_011518360.1:n.-436+52241T>C |
| XM_011520059.1:c.-436+52241T>C (OR2AG2) | XP_011518361.1:n.-436+52241T>C |
| XM_011520060.1:c.-436+52241T>C (OR2AG2) | XP_011518362.1:n.-436+52241T>C |
| XM_011520061.1:c.-435-76361T>C (OR2AG2) | XP_011518363.1:n.-435-76361T>C |