Linked Data
dbSNP Id:
rs2110726
gnomAD v2:
2-102794282-G-A
gnomAD v3:
2-102177822-G-A
gnomAD v4:
2-102177822-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.102177822G>A , CM000664.2:g.102177822G>A | GRCh38 |
| NC_000002.11:g.102794282G>A , CM000664.1:g.102794282G>A | GRCh37 |
| NC_000002.10:g.102160714G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000410023.6:c.*1063G>A (IL1R1) MANE Select | ENSP00000386380.1:n.*1063G>A | |
| ENST00000409589.5:c.*585G>A (IL1R1) | ENSP00000386555.1:n.*585G>A | |
| ENST00000410023.5:c.*1063G>A (IL1R1) | ENSP00000386380.1:n.*1063G>A | |
| NM_000877.3:c.*1063G>A (IL1R1) | NP_000868.1:n.*1063G>A | |
| NM_001288706.1:c.*1063G>A (IL1R1) | NP_001275635.1:n.*1063G>A | |
| XM_005263929.1:c.*1063G>A (IL1R1) | XP_005263986.1:n.*1063G>A | |
| XM_005263930.3:c.*1063G>A (IL1R1) | XP_005263987.1:n.*1063G>A | |
| XM_005263931.1:c.*1063G>A (IL1R1) | XP_005263988.1:n.*1063G>A | |
| XM_005263932.1:c.*1063G>A (IL1R1) | XP_005263989.1:n.*1063G>A | |
| XM_005263933.3:c.*1063G>A (IL1R1) | XP_005263990.1:n.*1063G>A | |
| XM_005263934.3:c.*1063G>A (IL1R1) | XP_005263991.1:n.*1063G>A | |
| XM_011511114.1:c.*1063G>A (IL1R1) | XP_011509416.1:n.*1063G>A | |
| XM_011511115.1:c.*1063G>A (IL1R1) | XP_011509417.1:n.*1063G>A | |
| XM_011511116.1:c.*1063G>A (IL1R1) | XP_011509418.1:n.*1063G>A | |
| XM_011511117.1:c.*1063G>A (IL1R1) | XP_011509419.1:n.*1063G>A | |
| XM_011511118.1:c.*1063G>A (IL1R1) | XP_011509420.1:n.*1063G>A | |
| XM_011511119.1:c.*1063G>A (IL1R1) | XP_011509421.1:n.*1063G>A | |
| NM_001320978.1:c.*1063G>A (IL1R1) | NP_001307907.1:n.*1063G>A | |
| NM_001320980.1:c.*1063G>A (IL1R1) | NP_001307909.1:n.*1063G>A | |
| NM_001320981.1:c.*1063G>A (IL1R1) | NP_001307910.1:n.*1063G>A | |
| NM_001320982.1:c.*1063G>A (IL1R1) | NP_001307911.1:n.*1063G>A | |
| NM_001320983.1:c.*1063G>A (IL1R1) | NP_001307912.1:n.*1063G>A | |
| NM_001320984.1:c.*1063G>A (IL1R1) | NP_001307913.1:n.*1063G>A | |
| NM_001320985.1:c.*1063G>A (IL1R1) | NP_001307914.1:n.*1063G>A | |
| XM_005263930.4:c.*1063G>A (IL1R1) | XP_005263987.1:n.*1063G>A | |
| XM_005263934.4:c.*1063G>A (IL1R1) | XP_005263991.1:n.*1063G>A | |
| XM_011511115.2:c.*1063G>A (IL1R1) | XP_011509417.1:n.*1063G>A | |
| XM_011511118.2:c.*1063G>A (IL1R1) | XP_011509420.1:n.*1063G>A | |
| XM_017003989.1:c.*1063G>A (IL1R1) | XP_016859478.1:n.*1063G>A | |
| NM_000877.4:c.*1063G>A (IL1R1) MANE Select | NP_000868.1:n.*1063G>A | |
| NM_001288706.2:c.*1063G>A (IL1R1) | NP_001275635.1:n.*1063G>A | |
| NM_001320978.2:c.*1063G>A (IL1R1) | NP_001307907.1:n.*1063G>A | |
| NM_001320980.2:c.*1063G>A (IL1R1) | NP_001307909.1:n.*1063G>A | |
| NM_001320981.2:c.*1063G>A (IL1R1) | NP_001307910.1:n.*1063G>A | |
| NM_001320982.2:c.*1063G>A (IL1R1) | NP_001307911.1:n.*1063G>A | |
| NR_174960.1:n.305+2090C>T (IL1R1-AS1) |