Revel Score:
ENST00000233954 (MANE Select)
0.045
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.102351615T>A , CM000664.2:g.102351615T>A | GRCh38 |
| NC_000002.11:g.102968075T>A , CM000664.1:g.102968075T>A | GRCh37 |
| NC_000002.10:g.102334507T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233954.6:c.1365T>A (IL1RL1) MANE Select | ENSP00000233954.1:p.Asn455Lys | |
| ENST00000233954.5:c.1365T>A (IL1RL1) | ENSP00000233954.1:p.Asn455Lys | |
| ENST00000410040.5:c.-28-11018T>A (IL18R1) | ENSP00000386663.1:n.-28-11018T>A | |
| NM_016232.4:c.1365T>A (IL1RL1) | NP_057316.3:p.Asn455Lys | |
| XM_006712839.2:c.1365T>A (IL1RL1) | XP_006712902.1:p.Asn455Lys | |
| XM_006712839.3:c.1365T>A (IL1RL1) | XP_006712902.1:p.Asn455Lys | |
| NM_016232.5:c.1365T>A (IL1RL1) MANE Select | NP_057316.3:p.Asn455Lys |