Linked Data
dbSNP Id:
rs12999542
gnomAD v2:
2-102965392-A-C
gnomAD v3:
2-102348932-A-C
gnomAD v4:
2-102348932-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.102348932A>C , CM000664.2:g.102348932A>C | GRCh38 |
| NC_000002.11:g.102965392A>C , CM000664.1:g.102965392A>C | GRCh37 |
| NC_000002.10:g.102331824A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000233954.6:c.1118-147A>C (IL1RL1) MANE Select | ENSP00000233954.1:n.1118-147A>C | |
| ENST00000233954.5:c.1118-147A>C (IL1RL1) | ENSP00000233954.1:n.1118-147A>C | |
| ENST00000410040.5:c.-28-13701A>C (IL18R1) | ENSP00000386663.1:n.-28-13701A>C | |
| NM_016232.4:c.1118-147A>C (IL1RL1) | NP_057316.3:n.1118-147A>C | |
| XM_006712839.2:c.1118-147A>C (IL1RL1) | XP_006712902.1:n.1118-147A>C | |
| XM_006712839.3:c.1118-147A>C (IL1RL1) | XP_006712902.1:n.1118-147A>C | |
| NM_016232.5:c.1118-147A>C (IL1RL1) MANE Select | NP_057316.3:n.1118-147A>C |