Canonical Allele Identifier: CA353248597

Gene: IL17RB ACTR8

Linked Data

• MyVariant Identifiers: chr3:g.53899094T>G (hg19) ; chr3:g.53865067T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53865067T>G , CM000665.2:g.53865067T>G	GRCh38
NC_000003.11:g.53899094T>G , CM000665.1:g.53899094T>G	GRCh37
NC_000003.10:g.53874134T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288167.8:c.1268T>G (IL17RB) MANE Select	ENSP00000288167.3:p.Phe423Cys
ENST00000288167.7:c.1268T>G (IL17RB)	ENSP00000288167.3:p.Phe423Cys
ENST00000475124.1:n.2301T>G (IL17RB)
NM_018725.3:c.1268T>G (IL17RB)	NP_061195.2:p.Phe423Cys
XM_005265310.3:c.1355T>G (IL17RB)	XP_005265367.1:p.Phe452Cys
XM_005265311.3:c.1307T>G (IL17RB)	XP_005265368.1:p.Phe436Cys
XM_005265312.3:c.1220T>G (IL17RB)	XP_005265369.1:p.Phe407Cys
XM_005265587.3:c.*46-48A>C (ACTR8)	XP_005265644.1:n.*46-48A>C
XM_011533940.1:c.1004T>G (IL17RB)	XP_011532242.1:p.Phe335Cys
XR_245147.3:n.1569T>G (IL17RB)
XR_940467.1:n.1434T>G (IL17RB)
XR_940468.1:n.1347T>G (IL17RB)
XM_005265310.5:c.1355T>G (IL17RB)	XP_005265367.1:p.Phe452Cys
XM_005265311.5:c.1307T>G (IL17RB)	XP_005265368.1:p.Phe436Cys
XM_005265312.5:c.1220T>G (IL17RB)	XP_005265369.1:p.Phe407Cys
XM_005265587.5:c.*46-48A>C (ACTR8)	XP_005265644.1:n.*46-48A>C
XM_011533941.3:c.*148T>G (IL17RB)	XP_011532243.1:n.*148T>G
XM_011534249.3:c.*3652A>C (ACTR8)	XP_011532551.1:n.*3652A>C
XM_017006804.2:c.1004T>G (IL17RB)	XP_016862293.1:p.Phe335Cys
XM_017006805.2:c.956T>G (IL17RB)	XP_016862294.1:p.Phe319Cys
XM_017006806.2:c.917T>G (IL17RB)	XP_016862295.1:p.Phe306Cys
XM_017006807.2:c.*148T>G (IL17RB)	XP_016862296.1:n.*148T>G
XR_940516.3:n.5605A>C (ACTR8)
NM_018725.4:c.1268T>G (IL17RB) MANE Select	NP_061195.2:p.Phe423Cys