Canonical Allele Identifier: CA353249182

Gene: IL17RB ACTR8

Linked Data

• MyVariant Identifiers: chr3:g.53899249T>G (hg19) ; chr3:g.53865222T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53865222T>G , CM000665.2:g.53865222T>G	GRCh38
NC_000003.11:g.53899249T>G , CM000665.1:g.53899249T>G	GRCh37
NC_000003.10:g.53874289T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288167.8:c.1423T>G (IL17RB) MANE Select	ENSP00000288167.3:p.Phe475Val
ENST00000288167.7:c.1423T>G (IL17RB)	ENSP00000288167.3:p.Phe475Val
ENST00000475124.1:n.2456T>G (IL17RB)
NM_018725.3:c.1423T>G (IL17RB)	NP_061195.2:p.Phe475Val
XM_005265310.3:c.1510T>G (IL17RB)	XP_005265367.1:p.Phe504Val
XM_005265311.3:c.1462T>G (IL17RB)	XP_005265368.1:p.Phe488Val
XM_005265312.3:c.1375T>G (IL17RB)	XP_005265369.1:p.Phe459Val
XM_005265587.3:c.*46-203A>C (ACTR8)	XP_005265644.1:n.*46-203A>C
XM_011533940.1:c.1159T>G (IL17RB)	XP_011532242.1:p.Phe387Val
XR_245147.3:n.1724T>G (IL17RB)
XR_940467.1:n.1589T>G (IL17RB)
XR_940468.1:n.1502T>G (IL17RB)
XM_005265310.5:c.1510T>G (IL17RB)	XP_005265367.1:p.Phe504Val
XM_005265311.5:c.1462T>G (IL17RB)	XP_005265368.1:p.Phe488Val
XM_005265312.5:c.1375T>G (IL17RB)	XP_005265369.1:p.Phe459Val
XM_005265587.5:c.*46-203A>C (ACTR8)	XP_005265644.1:n.*46-203A>C
XM_011533941.3:c.*303T>G (IL17RB)	XP_011532243.1:n.*303T>G
XM_011534249.3:c.*3497A>C (ACTR8)	XP_011532551.1:n.*3497A>C
XM_017006804.2:c.1159T>G (IL17RB)	XP_016862293.1:p.Phe387Val
XM_017006805.2:c.1111T>G (IL17RB)	XP_016862294.1:p.Phe371Val
XM_017006806.2:c.1072T>G (IL17RB)	XP_016862295.1:p.Phe358Val
XM_017006807.2:c.*303T>G (IL17RB)	XP_016862296.1:n.*303T>G
XR_940516.3:n.5450A>C (ACTR8)
NM_018725.4:c.1423T>G (IL17RB) MANE Select	NP_061195.2:p.Phe475Val