Canonical Allele Identifier: CA1365513636

Gene: IL17RB ACTR8

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288167.8:c.1255T= (IL17RB) MANE Select	ENSP00000288167.3:p.Ser419=
ENST00000288167.7:c.1255T= (IL17RB)	ENSP00000288167.3:p.Ser419=
ENST00000475124.1:n.2288T= (IL17RB)
NM_018725.3:c.1255T= (IL17RB)	NP_061195.2:p.Ser419=
XM_005265310.3:c.1342T= (IL17RB)	XP_005265367.1:p.Ser448=
XM_005265311.3:c.1294T= (IL17RB)	XP_005265368.1:p.Ser432=
XM_005265312.3:c.1207T= (IL17RB)	XP_005265369.1:p.Ser403=
XM_005265587.3:c.*46-35A= (ACTR8)	XP_005265644.1:n.*46-35A=
XM_011533940.1:c.991T= (IL17RB)	XP_011532242.1:p.Ser331=
XR_245147.3:n.1556T= (IL17RB)
XR_940467.1:n.1421T= (IL17RB)
XR_940468.1:n.1334T= (IL17RB)
XM_005265310.5:c.1342T= (IL17RB)	XP_005265367.1:p.Ser448=
XM_005265311.5:c.1294T= (IL17RB)	XP_005265368.1:p.Ser432=
XM_005265312.5:c.1207T= (IL17RB)	XP_005265369.1:p.Ser403=
XM_005265587.5:c.*46-35A= (ACTR8)	XP_005265644.1:n.*46-35A=
XM_011533941.3:c.*135T= (IL17RB)	XP_011532243.1:n.*135T=
XM_011534249.3:c.*3665A= (ACTR8)	XP_011532551.1:n.*3665A=
XM_017006804.2:c.991T= (IL17RB)	XP_016862293.1:p.Ser331=
XM_017006805.2:c.943T= (IL17RB)	XP_016862294.1:p.Ser315=
XM_017006806.2:c.904T= (IL17RB)	XP_016862295.1:p.Ser302=
XM_017006807.2:c.*135T= (IL17RB)	XP_016862296.1:n.*135T=
XR_940516.3:n.5618A= (ACTR8)
NM_018725.4:c.1255T= (IL17RB) MANE Select	NP_061195.2:p.Ser419=