Linked Data
dbSNP Id:
rs148083085
gnomAD v2:
3-8808375-T-C
gnomAD v3:
3-8766689-T-C
gnomAD v4:
3-8766689-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8766689T>C , CM000665.2:g.8766689T>C | GRCh38 |
| NC_000003.11:g.8808375T>C , CM000665.1:g.8808375T>C | GRCh37 |
| NC_000003.10:g.8783375T>C | NCBI36 |
| NG_008797.2:g.37880T>C , LRG_329:g.37880T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316793.8:c.922+577A>G (OXTR) MANE Select | ENSP00000324270.2:n.922+577A>G | |
| ENST00000316793.7:c.922+577A>G (OXTR) | ENSP00000324270.2:n.922+577A>G | |
| ENST00000472766.1:n.156-10788T>C (CAV3) | ||
| NM_000916.3:c.922+577A>G (OXTR) | NP_000907.2:n.922+577A>G | |
| XM_011533762.1:c.922+577A>G (OXTR) | XP_011532064.1:n.922+577A>G | |
| XM_011533763.1:c.922+577A>G (OXTR) | XP_011532065.1:n.922+577A>G | |
| NM_001354653.1:c.922+577A>G (OXTR) | NP_001341582.1:n.922+577A>G | |
| NM_001354654.1:c.922+577A>G (OXTR) | NP_001341583.1:n.922+577A>G | |
| NM_001354655.1:c.922+577A>G (OXTR) | NP_001341584.1:n.922+577A>G | |
| NM_001354656.1:c.922+577A>G (OXTR) | NP_001341585.1:n.922+577A>G | |
| NM_001354656.2:c.922+577A>G (OXTR) | NP_001341585.1:n.922+577A>G | |
| NM_000916.4:c.922+577A>G (OXTR) MANE Select | NP_000907.2:n.922+577A>G | |
| NM_001354653.2:c.922+577A>G (OXTR) | NP_001341582.1:n.922+577A>G | |
| NM_001354654.2:c.922+577A>G (OXTR) | NP_001341583.1:n.922+577A>G | |
| NM_001354655.2:c.922+577A>G (OXTR) | NP_001341584.1:n.922+577A>G | |
| NM_001354656.3:c.922+577A>G (OXTR) | NP_001341585.1:n.922+577A>G |