Canonical Allele Identifier: CA353248982

Gene: IL17RB ACTR8

Linked Data

• MyVariant Identifiers: chr3:g.53899195T>A (hg19) ; chr3:g.53865168T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53865168T>A , CM000665.2:g.53865168T>A	GRCh38
NC_000003.11:g.53899195T>A , CM000665.1:g.53899195T>A	GRCh37
NC_000003.10:g.53874235T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288167.8:c.1369T>A (IL17RB) MANE Select	ENSP00000288167.3:p.Tyr457Asn
ENST00000288167.7:c.1369T>A (IL17RB)	ENSP00000288167.3:p.Tyr457Asn
ENST00000475124.1:n.2402T>A (IL17RB)
NM_018725.3:c.1369T>A (IL17RB)	NP_061195.2:p.Tyr457Asn
XM_005265310.3:c.1456T>A (IL17RB)	XP_005265367.1:p.Tyr486Asn
XM_005265311.3:c.1408T>A (IL17RB)	XP_005265368.1:p.Tyr470Asn
XM_005265312.3:c.1321T>A (IL17RB)	XP_005265369.1:p.Tyr441Asn
XM_005265587.3:c.*46-149A>T (ACTR8)	XP_005265644.1:n.*46-149A>T
XM_011533940.1:c.1105T>A (IL17RB)	XP_011532242.1:p.Tyr369Asn
XR_245147.3:n.1670T>A (IL17RB)
XR_940467.1:n.1535T>A (IL17RB)
XR_940468.1:n.1448T>A (IL17RB)
XM_005265310.5:c.1456T>A (IL17RB)	XP_005265367.1:p.Tyr486Asn
XM_005265311.5:c.1408T>A (IL17RB)	XP_005265368.1:p.Tyr470Asn
XM_005265312.5:c.1321T>A (IL17RB)	XP_005265369.1:p.Tyr441Asn
XM_005265587.5:c.*46-149A>T (ACTR8)	XP_005265644.1:n.*46-149A>T
XM_011533941.3:c.*249T>A (IL17RB)	XP_011532243.1:n.*249T>A
XM_011534249.3:c.*3551A>T (ACTR8)	XP_011532551.1:n.*3551A>T
XM_017006804.2:c.1105T>A (IL17RB)	XP_016862293.1:p.Tyr369Asn
XM_017006805.2:c.1057T>A (IL17RB)	XP_016862294.1:p.Tyr353Asn
XM_017006806.2:c.1018T>A (IL17RB)	XP_016862295.1:p.Tyr340Asn
XM_017006807.2:c.*249T>A (IL17RB)	XP_016862296.1:n.*249T>A
XR_940516.3:n.5504A>T (ACTR8)
NM_018725.4:c.1369T>A (IL17RB) MANE Select	NP_061195.2:p.Tyr457Asn