MyVariant.info:
GRCh38
chr15:g.22081283T>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.22081283T>G , CM000677.2:g.22081283T>G | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614722.3:c.659T>G (OR4M2) MANE Select | ENSP00000483239.1:p.Phe220Cys | |
| ENST00000614722.2:c.659T>G (OR4M2) | ENSP00000483239.1:p.Phe220Cys | |
| ENST00000638815.1:n.512+182T>G (OR4M2) | ||
| ENST00000639059.1:c.-9-13230T>G (OR4M2-OT1) | ENSP00000493899.1:n.-9-13230T>G | |
| ENST00000614722.1:c.659T>G (OR4M2) | ENSP00000483239.1:p.Phe220Cys | |
| NM_001004719.2:c.659T>G (OR4M2) MANE Select | NP_001004719.2:p.Phe220Cys | |
| NR_110480.1:n.824-13230T>G (OR4M2-OT1) | ||
| NR_110481.1:n.556-13230T>G (OR4M2-OT1) |