Canonical Allele Identifier: CA353249025

Gene: IL17RB ACTR8

Linked Data

• MyVariant Identifiers: chr3:g.53899205T>G (hg19) ; chr3:g.53865178T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53865178T>G , CM000665.2:g.53865178T>G	GRCh38
NC_000003.11:g.53899205T>G , CM000665.1:g.53899205T>G	GRCh37
NC_000003.10:g.53874245T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288167.8:c.1379T>G (IL17RB) MANE Select	ENSP00000288167.3:p.Leu460Arg
ENST00000288167.7:c.1379T>G (IL17RB)	ENSP00000288167.3:p.Leu460Arg
ENST00000475124.1:n.2412T>G (IL17RB)
NM_018725.3:c.1379T>G (IL17RB)	NP_061195.2:p.Leu460Arg
XM_005265310.3:c.1466T>G (IL17RB)	XP_005265367.1:p.Leu489Arg
XM_005265311.3:c.1418T>G (IL17RB)	XP_005265368.1:p.Leu473Arg
XM_005265312.3:c.1331T>G (IL17RB)	XP_005265369.1:p.Leu444Arg
XM_005265587.3:c.*46-159A>C (ACTR8)	XP_005265644.1:n.*46-159A>C
XM_011533940.1:c.1115T>G (IL17RB)	XP_011532242.1:p.Leu372Arg
XR_245147.3:n.1680T>G (IL17RB)
XR_940467.1:n.1545T>G (IL17RB)
XR_940468.1:n.1458T>G (IL17RB)
XM_005265310.5:c.1466T>G (IL17RB)	XP_005265367.1:p.Leu489Arg
XM_005265311.5:c.1418T>G (IL17RB)	XP_005265368.1:p.Leu473Arg
XM_005265312.5:c.1331T>G (IL17RB)	XP_005265369.1:p.Leu444Arg
XM_005265587.5:c.*46-159A>C (ACTR8)	XP_005265644.1:n.*46-159A>C
XM_011533941.3:c.*259T>G (IL17RB)	XP_011532243.1:n.*259T>G
XM_011534249.3:c.*3541A>C (ACTR8)	XP_011532551.1:n.*3541A>C
XM_017006804.2:c.1115T>G (IL17RB)	XP_016862293.1:p.Leu372Arg
XM_017006805.2:c.1067T>G (IL17RB)	XP_016862294.1:p.Leu356Arg
XM_017006806.2:c.1028T>G (IL17RB)	XP_016862295.1:p.Leu343Arg
XM_017006807.2:c.*259T>G (IL17RB)	XP_016862296.1:n.*259T>G
XR_940516.3:n.5494A>C (ACTR8)
NM_018725.4:c.1379T>G (IL17RB) MANE Select	NP_061195.2:p.Leu460Arg