Canonical Allele Identifier: CA353248650
Gene: IL17RB HGNC NCBI
ACTR8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53865081A>T , CM000665.2:g.53865081A>T GRCh38
NC_000003.11:g.53899108A>T , CM000665.1:g.53899108A>T GRCh37
NC_000003.10:g.53874148A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288167.8:c.1282A>T (IL17RB) MANE Select ENSP00000288167.3:p.Asn428Tyr
ENST00000288167.7:c.1282A>T (IL17RB) ENSP00000288167.3:p.Asn428Tyr
ENST00000475124.1:n.2315A>T (IL17RB)
NM_018725.3:c.1282A>T (IL17RB) NP_061195.2:p.Asn428Tyr
XM_005265310.3:c.1369A>T (IL17RB) XP_005265367.1:p.Asn457Tyr
XM_005265311.3:c.1321A>T (IL17RB) XP_005265368.1:p.Asn441Tyr
XM_005265312.3:c.1234A>T (IL17RB) XP_005265369.1:p.Asn412Tyr
XM_005265587.3:c.*46-62T>A (ACTR8) XP_005265644.1:n.*46-62T>A
XM_011533940.1:c.1018A>T (IL17RB) XP_011532242.1:p.Asn340Tyr
XR_245147.3:n.1583A>T (IL17RB)
XR_940467.1:n.1448A>T (IL17RB)
XR_940468.1:n.1361A>T (IL17RB)
XM_005265310.5:c.1369A>T (IL17RB) XP_005265367.1:p.Asn457Tyr
XM_005265311.5:c.1321A>T (IL17RB) XP_005265368.1:p.Asn441Tyr
XM_005265312.5:c.1234A>T (IL17RB) XP_005265369.1:p.Asn412Tyr
XM_005265587.5:c.*46-62T>A (ACTR8) XP_005265644.1:n.*46-62T>A
XM_011533941.3:c.*162A>T (IL17RB) XP_011532243.1:n.*162A>T
XM_011534249.3:c.*3638T>A (ACTR8) XP_011532551.1:n.*3638T>A
XM_017006804.2:c.1018A>T (IL17RB) XP_016862293.1:p.Asn340Tyr
XM_017006805.2:c.970A>T (IL17RB) XP_016862294.1:p.Asn324Tyr
XM_017006806.2:c.931A>T (IL17RB) XP_016862295.1:p.Asn311Tyr
XM_017006807.2:c.*162A>T (IL17RB) XP_016862296.1:n.*162A>T
XR_940516.3:n.5591T>A (ACTR8)
NM_018725.4:c.1282A>T (IL17RB) MANE Select NP_061195.2:p.Asn428Tyr