Linked Data
dbSNP Id:
rs10208293
gnomAD v2:
2-102966310-G-A
gnomAD v3:
2-102349850-G-A
gnomAD v4:
2-102349850-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.102349850G>A , CM000664.2:g.102349850G>A | GRCh38 |
| NC_000002.11:g.102966310G>A , CM000664.1:g.102966310G>A | GRCh37 |
| NC_000002.10:g.102332742G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000233954.6:c.1285+604G>A (IL1RL1) MANE Select | ENSP00000233954.1:n.1285+604G>A | |
| ENST00000233954.5:c.1285+604G>A (IL1RL1) | ENSP00000233954.1:n.1285+604G>A | |
| ENST00000410040.5:c.-28-12783G>A (IL18R1) | ENSP00000386663.1:n.-28-12783G>A | |
| NM_016232.4:c.1285+604G>A (IL1RL1) | NP_057316.3:n.1285+604G>A | |
| XM_006712839.2:c.1285+604G>A (IL1RL1) | XP_006712902.1:n.1285+604G>A | |
| XM_006712839.3:c.1285+604G>A (IL1RL1) | XP_006712902.1:n.1285+604G>A | |
| NM_016232.5:c.1285+604G>A (IL1RL1) MANE Select | NP_057316.3:n.1285+604G>A |