Linked Data
dbSNP Id:
rs1160630933
gnomAD v2:
1-67672656-T-C
gnomAD v3:
1-67206973-T-C
gnomAD v4:
1-67206973-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.67206973T>C , CM000663.2:g.67206973T>C | GRCh38 |
| NC_000001.10:g.67672656T>C , CM000663.1:g.67672656T>C | GRCh37 |
| NC_000001.9:g.67445244T>C | NCBI36 |
| NG_011498.1:g.45488T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000697148.1:c.592T>C (IL23R) | ENSP00000513137.1:n.592T>C | |
| ENST00000697149.1:c.555T>C (IL23R) | ENSP00000513138.1:n.555T>C | |
| ENST00000697150.1:c.716T>C (IL23R) | ENSP00000513139.1:p.Ile239Thr | |
| ENST00000697151.1:c.716T>C (IL23R) | ENSP00000513140.1:p.Ile239Thr | |
| ENST00000697152.1:c.716T>C (IL23R) | ENSP00000513141.1:p.Ile239Thr | |
| ENST00000697153.1:c.555T>C (IL23R) | ENSP00000513142.1:n.555T>C | |
| ENST00000697154.1:c.716T>C (IL23R) | ENSP00000513143.1:p.Ile239Thr | |
| ENST00000697155.1:c.492-12601T>C (IL23R) | ENSP00000513144.1:n.492-12601T>C | |
| ENST00000697156.1:c.716T>C (IL23R) | ENSP00000513145.1:p.Ile239Thr | |
| ENST00000697157.1:c.652+6076T>C (IL23R) | ENSP00000513146.1:n.652+6076T>C | |
| ENST00000697158.1:c.716T>C (IL23R) | ENSP00000513147.1:p.Ile239Thr | |
| ENST00000697159.1:c.492-12601T>C (IL23R) | ENSP00000513148.1:n.492-12601T>C | |
| ENST00000697160.1:c.716T>C (IL23R) | ENSP00000513149.1:p.Ile239Thr | |
| ENST00000697161.1:c.491+24014T>C (IL23R) | ENSP00000513150.1:n.491+24014T>C | |
| ENST00000697162.1:c.645T>C (IL23R) | ENSP00000513151.1:n.645T>C | |
| ENST00000697163.1:c.716T>C (IL23R) | ENSP00000513152.1:p.Ile239Thr | |
| ENST00000697164.1:c.716T>C (IL23R) | ENSP00000513153.1:p.Ile239Thr | |
| ENST00000697165.1:c.652+6076T>C (IL23R) | ENSP00000513154.1:n.652+6076T>C | |
| ENST00000697223.1:c.555T>C (IL23R) | ENSP00000513190.1:n.555T>C | |
| ENST00000697224.1:c.555T>C (IL23R) | ENSP00000513191.1:n.555T>C | |
| ENST00000697225.1:c.492-12601T>C (IL23R) | ENSP00000513192.1:n.492-12601T>C | |
| ENST00000697226.1:c.492-12601T>C (IL23R) | ENSP00000513193.1:n.492-12601T>C | |
| ENST00000697227.1:c.716T>C (IL23R) | ENSP00000513194.1:p.Ile239Thr | |
| ENST00000697228.1:c.647+6076T>C (IL23R) | ENSP00000513195.1:n.647+6076T>C | |
| ENST00000697229.1:c.645T>C (IL23R) | ENSP00000513196.1:n.645T>C | |
| ENST00000697230.1:c.716T>C (IL23R) | ENSP00000513197.1:p.Ile239Thr | |
| ENST00000697231.1:c.711T>C (IL23R) | ENSP00000513198.1:n.711T>C | |
| ENST00000697232.1:c.645T>C (IL23R) | ENSP00000513199.1:n.645T>C | |
| ENST00000347310.10:c.716T>C (IL23R) MANE Select | ENSP00000321345.5:p.Ile239Thr | |
| ENST00000637002.1:c.107T>C (IL23R) | ENSP00000490340.1:p.Ile36Thr | |
| ENST00000347310.9:c.716T>C (IL23R) | ENSP00000321345.5:p.Ile239Thr | |
| ENST00000371007.6:c.-104+24873A>G (C1orf141) | ENSP00000360046.1:n.-104+24873A>G | |
| ENST00000448166.6:c.-104+24873A>G (C1orf141) | ENSP00000415519.2:n.-104+24873A>G | |
| NM_144701.2:c.716T>C (IL23R) | NP_653302.2:p.Ile239Thr | |
| XM_005270516.2:c.-47T>C (IL23R) | XP_005270573.1:n.-47T>C | |
| XM_011540789.1:c.806T>C (IL23R) | XP_011539091.1:p.Ile269Thr | |
| XM_011540790.1:c.716T>C (IL23R) | XP_011539092.1:p.Ile239Thr | |
| XM_011540791.1:c.716T>C (IL23R) | XP_011539093.1:p.Ile239Thr | |
| XM_011540790.3:c.716T>C (IL23R) | XP_011539092.1:p.Ile239Thr | |
| XM_011540791.3:c.716T>C (IL23R) | XP_011539093.1:p.Ile239Thr | |
| XR_001736993.1:n.899T>C (IL23R) | ||
| NM_144701.3:c.716T>C (IL23R) MANE Select | NP_653302.2:p.Ile239Thr |