Canonical Allele Identifier: CA353248548
Gene: IL17RB HGNC NCBI
ACTR8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53865054T>A , CM000665.2:g.53865054T>A GRCh38
NC_000003.11:g.53899081T>A , CM000665.1:g.53899081T>A GRCh37
NC_000003.10:g.53874121T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288167.8:c.1255T>A (IL17RB) MANE Select ENSP00000288167.3:p.Ser419Thr
ENST00000288167.7:c.1255T>A (IL17RB) ENSP00000288167.3:p.Ser419Thr
ENST00000475124.1:n.2288T>A (IL17RB)
NM_018725.3:c.1255T>A (IL17RB) NP_061195.2:p.Ser419Thr
XM_005265310.3:c.1342T>A (IL17RB) XP_005265367.1:p.Ser448Thr
XM_005265311.3:c.1294T>A (IL17RB) XP_005265368.1:p.Ser432Thr
XM_005265312.3:c.1207T>A (IL17RB) XP_005265369.1:p.Ser403Thr
XM_005265587.3:c.*46-35A>T (ACTR8) XP_005265644.1:n.*46-35A>T
XM_011533940.1:c.991T>A (IL17RB) XP_011532242.1:p.Ser331Thr
XR_245147.3:n.1556T>A (IL17RB)
XR_940467.1:n.1421T>A (IL17RB)
XR_940468.1:n.1334T>A (IL17RB)
XM_005265310.5:c.1342T>A (IL17RB) XP_005265367.1:p.Ser448Thr
XM_005265311.5:c.1294T>A (IL17RB) XP_005265368.1:p.Ser432Thr
XM_005265312.5:c.1207T>A (IL17RB) XP_005265369.1:p.Ser403Thr
XM_005265587.5:c.*46-35A>T (ACTR8) XP_005265644.1:n.*46-35A>T
XM_011533941.3:c.*135T>A (IL17RB) XP_011532243.1:n.*135T>A
XM_011534249.3:c.*3665A>T (ACTR8) XP_011532551.1:n.*3665A>T
XM_017006804.2:c.991T>A (IL17RB) XP_016862293.1:p.Ser331Thr
XM_017006805.2:c.943T>A (IL17RB) XP_016862294.1:p.Ser315Thr
XM_017006806.2:c.904T>A (IL17RB) XP_016862295.1:p.Ser302Thr
XM_017006807.2:c.*135T>A (IL17RB) XP_016862296.1:n.*135T>A
XR_940516.3:n.5618A>T (ACTR8)
NM_018725.4:c.1255T>A (IL17RB) MANE Select NP_061195.2:p.Ser419Thr