Linked Data
dbSNP Id:
rs72921001
gnomAD v2:
11-6889648-C-A
gnomAD v3:
11-6868417-C-A
gnomAD v4:
11-6868417-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6868417C>A , CM000673.2:g.6868417C>A | GRCh38 |
| NC_000011.9:g.6889648C>A , CM000673.1:g.6889648C>A | GRCh37 |
| NC_000011.8:g.6846224C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000641461.1:c.-132-1206C>A (OR10A2) MANE Select | ENSP00000493131.1:n.-132-1206C>A | |
| XM_011520058.1:c.-436+29676G>T (OR2AG2) | XP_011518360.1:n.-436+29676G>T | |
| XM_011520059.1:c.-436+29676G>T (OR2AG2) | XP_011518361.1:n.-436+29676G>T | |
| XM_011520060.1:c.-436+29676G>T (OR2AG2) | XP_011518362.1:n.-436+29676G>T | |
| XM_011520061.1:c.-436+56081G>T (OR2AG2) | XP_011518363.1:n.-436+56081G>T | |
| NM_001004460.2:c.-132-1206C>A (OR10A2) MANE Select | NP_001004460.1:n.-132-1206C>A |