Revel Score:
ENST00000288167 (MANE Select)
0.037
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.53865249C>A , CM000665.2:g.53865249C>A | GRCh38 |
| NC_000003.11:g.53899276C>A , CM000665.1:g.53899276C>A | GRCh37 |
| NC_000003.10:g.53874316C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000288167.8:c.1450C>A (IL17RB) MANE Select | ENSP00000288167.3:p.Gln484Lys | |
| ENST00000288167.7:c.1450C>A (IL17RB) | ENSP00000288167.3:p.Gln484Lys | |
| ENST00000475124.1:n.2483C>A (IL17RB) | ||
| NM_018725.3:c.1450C>A (IL17RB) | NP_061195.2:p.Gln484Lys | |
| XM_005265310.3:c.1537C>A (IL17RB) | XP_005265367.1:p.Gln513Lys | |
| XM_005265311.3:c.1489C>A (IL17RB) | XP_005265368.1:p.Gln497Lys | |
| XM_005265312.3:c.1402C>A (IL17RB) | XP_005265369.1:p.Gln468Lys | |
| XM_005265587.3:c.*46-230G>T (ACTR8) | XP_005265644.1:n.*46-230G>T | |
| XM_011533940.1:c.1186C>A (IL17RB) | XP_011532242.1:p.Gln396Lys | |
| XR_245147.3:n.1751C>A (IL17RB) | ||
| XR_940467.1:n.1616C>A (IL17RB) | ||
| XR_940468.1:n.1529C>A (IL17RB) | ||
| XM_005265310.5:c.1537C>A (IL17RB) | XP_005265367.1:p.Gln513Lys | |
| XM_005265311.5:c.1489C>A (IL17RB) | XP_005265368.1:p.Gln497Lys | |
| XM_005265312.5:c.1402C>A (IL17RB) | XP_005265369.1:p.Gln468Lys | |
| XM_005265587.5:c.*46-230G>T (ACTR8) | XP_005265644.1:n.*46-230G>T | |
| XM_011533941.3:c.*330C>A (IL17RB) | XP_011532243.1:n.*330C>A | |
| XM_011534249.3:c.*3470G>T (ACTR8) | XP_011532551.1:n.*3470G>T | |
| XM_017006804.2:c.1186C>A (IL17RB) | XP_016862293.1:p.Gln396Lys | |
| XM_017006805.2:c.1138C>A (IL17RB) | XP_016862294.1:p.Gln380Lys | |
| XM_017006806.2:c.1099C>A (IL17RB) | XP_016862295.1:p.Gln367Lys | |
| XM_017006807.2:c.*330C>A (IL17RB) | XP_016862296.1:n.*330C>A | |
| XR_940516.3:n.5423G>T (ACTR8) | ||
| NM_018725.4:c.1450C>A (IL17RB) MANE Select | NP_061195.2:p.Gln484Lys |