Linked Data
dbSNP Id:
rs1420101
ExAC:
2:102957716 C / T
gnomAD v2:
2-102957716-C-T
gnomAD v3:
2-102341256-C-T
gnomAD v4:
2-102341256-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.102341256C>T , CM000664.2:g.102341256C>T | GRCh38 |
| NC_000002.11:g.102957716C>T , CM000664.1:g.102957716C>T | GRCh37 |
| NC_000002.10:g.102324148C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000233954.6:c.610+428C>T (IL1RL1) MANE Select | ENSP00000233954.1:n.610+428C>T | |
| ENST00000233954.5:c.610+428C>T (IL1RL1) | ENSP00000233954.1:n.610+428C>T | |
| ENST00000311734.6:c.610+428C>T (IL1RL1) | ENSP00000310371.2:n.610+428C>T | |
| ENST00000404917.6:c.259+428C>T (IL1RL1) | ENSP00000384822.2:n.259+428C>T | |
| ENST00000409584.5:c.610+428C>T (IL1RL1) | ENSP00000386618.1:n.610+428C>T | |
| ENST00000410040.5:c.-28-21377C>T (IL18R1) | ENSP00000386663.1:n.-28-21377C>T | |
| ENST00000427077.1:c.679C>T (IL1RL1) | ENSP00000391120.1:p.Leu227= | |
| ENST00000482701.5:n.444-967C>T (IL1RL1) | ||
| NM_001282408.1:c.259+428C>T (IL1RL1) | NP_001269337.1:n.259+428C>T | |
| NM_003856.3:c.610+428C>T (IL1RL1) | NP_003847.2:n.610+428C>T | |
| NM_016232.4:c.610+428C>T (IL1RL1) | NP_057316.3:n.610+428C>T | |
| NR_104167.1:n.916C>T (IL1RL1) | ||
| XM_006712839.2:c.610+428C>T (IL1RL1) | XP_006712902.1:n.610+428C>T | |
| XM_011512151.1:c.610+428C>T (IL1RL1) | XP_011510453.1:n.610+428C>T | |
| XM_006712839.3:c.610+428C>T (IL1RL1) | XP_006712902.1:n.610+428C>T | |
| NM_003856.4:c.610+428C>T (IL1RL1) | NP_003847.2:n.610+428C>T | |
| NM_016232.5:c.610+428C>T (IL1RL1) MANE Select | NP_057316.3:n.610+428C>T | |
| NR_104167.2:n.909C>T (IL1RL1) | ||
| NM_001282408.2:c.259+428C>T (IL1RL1) | NP_001269337.1:n.259+428C>T |