Linked Data
dbSNP Id:
rs17639215
gnomAD v2:
2-102953444-G-A
gnomAD v3:
2-102336984-G-A
gnomAD v4:
2-102336984-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.102336984G>A , CM000664.2:g.102336984G>A | GRCh38 |
| NC_000002.11:g.102953444G>A , CM000664.1:g.102953444G>A | GRCh37 |
| NC_000002.10:g.102319876G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000233954.6:c.-149-1132G>A (IL1RL1) MANE Select | ENSP00000233954.1:n.-149-1132G>A | |
| ENST00000233954.5:c.-149-1132G>A (IL1RL1) | ENSP00000233954.1:n.-149-1132G>A | |
| ENST00000404917.6:c.-146-1997G>A (IL1RL1) | ENSP00000384822.2:n.-146-1997G>A | |
| ENST00000410040.5:c.-29+25361G>A (IL18R1) | ENSP00000386663.1:n.-29+25361G>A | |
| ENST00000447231.5:c.-149-1132G>A (IL1RL1) | ENSP00000409437.1:n.-149-1132G>A | |
| ENST00000473175.1:n.96-1132G>A (IL1RL1) | ||
| NM_001282408.1:c.-146-1997G>A (IL1RL1) | NP_001269337.1:n.-146-1997G>A | |
| NM_016232.4:c.-149-1132G>A (IL1RL1) | NP_057316.3:n.-149-1132G>A | |
| XM_011512151.1:c.-149-1132G>A (IL1RL1) | XP_011510453.1:n.-149-1132G>A | |
| NM_016232.5:c.-149-1132G>A (IL1RL1) MANE Select | NP_057316.3:n.-149-1132G>A | |
| NM_001282408.2:c.-146-1997G>A (IL1RL1) | NP_001269337.1:n.-146-1997G>A |