Linked Data
dbSNP Id:
rs3831817
gnomAD v2:
3-8808428-G-GC
gnomAD v3:
3-8766742-G-GC
gnomAD v4:
3-8766742-G-GC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8766744dup , CM000665.2:g.8766744dup | GRCh38 |
| NC_000003.11:g.8808430dup , CM000665.1:g.8808430dup | GRCh37 |
| NC_000003.10:g.8783430dup | NCBI36 |
| NG_008797.2:g.37935dup , LRG_329:g.37935dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000316793.8:c.922+523dup (OXTR) MANE Select | ENSP00000324270.2:n.922+523dup | |
| ENST00000316793.7:c.922+523dup (OXTR) | ENSP00000324270.2:n.922+523dup | |
| ENST00000472766.1:n.156-10733dup (CAV3) | ||
| NM_000916.3:c.922+523dup (OXTR) | NP_000907.2:n.922+523dup | |
| XM_011533762.1:c.922+523dup (OXTR) | XP_011532064.1:n.922+523dup | |
| XM_011533763.1:c.922+523dup (OXTR) | XP_011532065.1:n.922+523dup | |
| NM_001354653.1:c.922+523dup (OXTR) | NP_001341582.1:n.922+523dup | |
| NM_001354654.1:c.922+523dup (OXTR) | NP_001341583.1:n.922+523dup | |
| NM_001354655.1:c.922+523dup (OXTR) | NP_001341584.1:n.922+523dup | |
| NM_001354656.1:c.922+523dup (OXTR) | NP_001341585.1:n.922+523dup | |
| NM_001354656.2:c.922+523dup (OXTR) | NP_001341585.1:n.922+523dup | |
| NM_000916.4:c.922+523dup (OXTR) MANE Select | NP_000907.2:n.922+523dup | |
| NM_001354653.2:c.922+523dup (OXTR) | NP_001341582.1:n.922+523dup | |
| NM_001354654.2:c.922+523dup (OXTR) | NP_001341583.1:n.922+523dup | |
| NM_001354655.2:c.922+523dup (OXTR) | NP_001341584.1:n.922+523dup | |
| NM_001354656.3:c.922+523dup (OXTR) | NP_001341585.1:n.922+523dup |