gnomAD v3:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.102348282C>G , CM000664.2:g.102348282C>G | GRCh38 |
| NC_000002.11:g.102964742C>G , CM000664.1:g.102964742C>G | GRCh37 |
| NC_000002.10:g.102331174C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233954.6:c.1117+191C>G (IL1RL1) MANE Select | ENSP00000233954.1:n.1117+191C>G | |
| ENST00000233954.5:c.1117+191C>G (IL1RL1) | ENSP00000233954.1:n.1117+191C>G | |
| ENST00000410040.5:c.-28-14351C>G (IL18R1) | ENSP00000386663.1:n.-28-14351C>G | |
| NM_016232.4:c.1117+191C>G (IL1RL1) | NP_057316.3:n.1117+191C>G | |
| XM_006712839.2:c.1117+191C>G (IL1RL1) | XP_006712902.1:n.1117+191C>G | |
| XM_006712839.3:c.1117+191C>G (IL1RL1) | XP_006712902.1:n.1117+191C>G | |
| NM_016232.5:c.1117+191C>G (IL1RL1) MANE Select | NP_057316.3:n.1117+191C>G |