gnomAD v3:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8769477A>C , CM000665.2:g.8769477A>C | GRCh38 |
| NC_000003.11:g.8811163A>C , CM000665.1:g.8811163A>C | GRCh37 |
| NC_000003.10:g.8786163A>C | NCBI36 |
| NG_008797.2:g.40668A>C , LRG_329:g.40668A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316793.8:c.-485T>G (OXTR) MANE Select | ENSP00000324270.2:n.-485T>G | |
| ENST00000316793.7:c.-485T>G (OXTR) | ENSP00000324270.2:n.-485T>G | |
| ENST00000431493.1:c.-462T>G (OXTR) | ENSP00000414828.1:n.-462T>G | |
| ENST00000472766.1:n.156-8000A>C (CAV3) | ||
| ENST00000474615.1:n.137T>G (OXTR) | ||
| NM_000916.3:c.-485T>G (OXTR) | NP_000907.2:n.-485T>G | |
| XM_011533762.1:c.-462T>G (OXTR) | XP_011532064.1:n.-462T>G | |
| XM_011533763.1:c.-238-886T>G (OXTR) | XP_011532065.1:n.-238-886T>G | |
| NM_001354653.1:c.-405T>G (OXTR) | NP_001341582.1:n.-405T>G | |
| NM_001354654.1:c.-462T>G (OXTR) | NP_001341583.1:n.-462T>G | |
| NM_000916.4:c.-485T>G (OXTR) MANE Select | NP_000907.2:n.-485T>G | |
| NM_001354653.2:c.-405T>G (OXTR) | NP_001341582.1:n.-405T>G | |
| NM_001354654.2:c.-462T>G (OXTR) | NP_001341583.1:n.-462T>G |