Canonical Allele Identifier: CA1365513721

Gene: IL17RB ACTR8

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53865249C= , CM000665.2:g.53865249C=	GRCh38
NC_000003.11:g.53899276C= , CM000665.1:g.53899276C=	GRCh37
NC_000003.10:g.53874316C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018725.4:c.1450C= (IL17RB) MANE Select	NP_061195.2:p.Gln484=
ENST00000288167.8:c.1450C= (IL17RB) MANE Select	ENSP00000288167.3:p.Gln484=
NM_018725.3:c.1450C= (IL17RB)	NP_061195.2:p.Gln484=
ENST00000288167.7:c.1450C= (IL17RB)	ENSP00000288167.3:p.Gln484=
ENST00000475124.1:n.2483C= (IL17RB)
XM_005265310.3:c.1537C= (IL17RB)	XP_005265367.1:p.Gln513=
XM_005265310.5:c.1537C= (IL17RB)	XP_005265367.1:p.Gln513=
XM_005265311.3:c.1489C= (IL17RB)	XP_005265368.1:p.Gln497=
XM_005265311.5:c.1489C= (IL17RB)	XP_005265368.1:p.Gln497=
XM_005265312.3:c.1402C= (IL17RB)	XP_005265369.1:p.Gln468=
XM_005265312.5:c.1402C= (IL17RB)	XP_005265369.1:p.Gln468=
XM_005265587.3:c.*46-230G= (ACTR8)	XP_005265644.1:n.*46-230G=
XM_005265587.5:c.*46-230G= (ACTR8)	XP_005265644.1:n.*46-230G=
XM_011533940.1:c.1186C= (IL17RB)	XP_011532242.1:p.Gln396=
XM_011533941.3:c.*330C= (IL17RB)	XP_011532243.1:n.*330C=
XM_011534249.3:c.*3470G= (ACTR8)	XP_011532551.1:n.*3470G=
XM_017006804.2:c.1186C= (IL17RB)	XP_016862293.1:p.Gln396=
XM_017006805.2:c.1138C= (IL17RB)	XP_016862294.1:p.Gln380=
XM_017006806.2:c.1099C= (IL17RB)	XP_016862295.1:p.Gln367=
XM_017006807.2:c.*330C= (IL17RB)	XP_016862296.1:n.*330C=
XR_245147.3:n.1751C= (IL17RB)
XR_940467.1:n.1616C= (IL17RB)
XR_940468.1:n.1529C= (IL17RB)
XR_940516.3:n.5423G= (ACTR8)