gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.37747654 (EAS)
Genomes Max Group AF
0.37747654 (EAS)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.102348872G>C , CM000664.2:g.102348872G>C | GRCh38 |
| NC_000002.11:g.102965332G>C , CM000664.1:g.102965332G>C | GRCh37 |
| NC_000002.10:g.102331764G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233954.6:c.1118-207G>C (IL1RL1) MANE Select | ENSP00000233954.1:n.1118-207G>C | |
| ENST00000233954.5:c.1118-207G>C (IL1RL1) | ENSP00000233954.1:n.1118-207G>C | |
| ENST00000410040.5:c.-28-13761G>C (IL18R1) | ENSP00000386663.1:n.-28-13761G>C | |
| NM_016232.4:c.1118-207G>C (IL1RL1) | NP_057316.3:n.1118-207G>C | |
| XM_006712839.2:c.1118-207G>C (IL1RL1) | XP_006712902.1:n.1118-207G>C | |
| XM_006712839.3:c.1118-207G>C (IL1RL1) | XP_006712902.1:n.1118-207G>C | |
| NM_016232.5:c.1118-207G>C (IL1RL1) MANE Select | NP_057316.3:n.1118-207G>C |