COSMIC:
COSM3757549 (not active)
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.70223249 (AFR)
Genomes Max Group AF
0.69546771 (AFR)
Exomes Max Group AF
0.70596111 (AFR)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.102351615T>C , CM000664.2:g.102351615T>C | GRCh38 |
| NC_000002.11:g.102968075T>C , CM000664.1:g.102968075T>C | GRCh37 |
| NC_000002.10:g.102334507T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233954.6:c.1365T>C (IL1RL1) MANE Select | ENSP00000233954.1:p.Asn455= | |
| ENST00000233954.5:c.1365T>C (IL1RL1) | ENSP00000233954.1:p.Asn455= | |
| ENST00000410040.5:c.-28-11018T>C (IL18R1) | ENSP00000386663.1:n.-28-11018T>C | |
| NM_016232.4:c.1365T>C (IL1RL1) | NP_057316.3:p.Asn455= | |
| XM_006712839.2:c.1365T>C (IL1RL1) | XP_006712902.1:p.Asn455= | |
| XM_006712839.3:c.1365T>C (IL1RL1) | XP_006712902.1:p.Asn455= | |
| NM_016232.5:c.1365T>C (IL1RL1) MANE Select | NP_057316.3:p.Asn455= |