Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.102349607G= , CM000664.2:g.102349607G= | GRCh38 |
| NC_000002.11:g.102966067G= , CM000664.1:g.102966067G= | GRCh37 |
| NC_000002.10:g.102332499G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_016232.5:c.1285+361G= (IL1RL1) MANE Select | NP_057316.3:n.1285+361G= |
| ENST00000233954.6:c.1285+361G= (IL1RL1) MANE Select | ENSP00000233954.1:n.1285+361G= |
| NM_016232.4:c.1285+361G= (IL1RL1) | NP_057316.3:n.1285+361G= |
| ENST00000233954.5:c.1285+361G= (IL1RL1) | ENSP00000233954.1:n.1285+361G= |
| ENST00000410040.5:c.-28-13026G= (IL18R1) | ENSP00000386663.1:n.-28-13026G= |
| XM_006712839.2:c.1285+361G= (IL1RL1) | XP_006712902.1:n.1285+361G= |
| XM_006712839.3:c.1285+361G= (IL1RL1) | XP_006712902.1:n.1285+361G= |