Canonical Allele Identifier: CA433896610

Gene: IL17RB ACTR8

Linked Data

• dbSNP Id: rs1237594194
• gnomAD v2: 3-53899080-C-T
• gnomAD v4: 3-53865053-C-T
• MyVariant Identifiers: chr3:g.53899080C>T (hg19) ; chr3:g.53865053C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53865053C>T , CM000665.2:g.53865053C>T	GRCh38
NC_000003.11:g.53899080C>T , CM000665.1:g.53899080C>T	GRCh37
NC_000003.10:g.53874120C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288167.8:c.1254C>T (IL17RB) MANE Select	ENSP00000288167.3:p.Asn418=
ENST00000288167.7:c.1254C>T (IL17RB)	ENSP00000288167.3:p.Asn418=
ENST00000475124.1:n.2287C>T (IL17RB)
NM_018725.3:c.1254C>T (IL17RB)	NP_061195.2:p.Asn418=
XM_005265310.3:c.1341C>T (IL17RB)	XP_005265367.1:p.Asn447=
XM_005265311.3:c.1293C>T (IL17RB)	XP_005265368.1:p.Asn431=
XM_005265312.3:c.1206C>T (IL17RB)	XP_005265369.1:p.Asn402=
XM_005265587.3:c.*46-34G>A (ACTR8)	XP_005265644.1:n.*46-34G>A
XM_011533940.1:c.990C>T (IL17RB)	XP_011532242.1:p.Asn330=
XR_245147.3:n.1555C>T (IL17RB)
XR_940467.1:n.1420C>T (IL17RB)
XR_940468.1:n.1333C>T (IL17RB)
XM_005265310.5:c.1341C>T (IL17RB)	XP_005265367.1:p.Asn447=
XM_005265311.5:c.1293C>T (IL17RB)	XP_005265368.1:p.Asn431=
XM_005265312.5:c.1206C>T (IL17RB)	XP_005265369.1:p.Asn402=
XM_005265587.5:c.*46-34G>A (ACTR8)	XP_005265644.1:n.*46-34G>A
XM_011533941.3:c.*134C>T (IL17RB)	XP_011532243.1:n.*134C>T
XM_011534249.3:c.*3666G>A (ACTR8)	XP_011532551.1:n.*3666G>A
XM_017006804.2:c.990C>T (IL17RB)	XP_016862293.1:p.Asn330=
XM_017006805.2:c.942C>T (IL17RB)	XP_016862294.1:p.Asn314=
XM_017006806.2:c.903C>T (IL17RB)	XP_016862295.1:p.Asn301=
XM_017006807.2:c.*134C>T (IL17RB)	XP_016862296.1:n.*134C>T
XR_940516.3:n.5619G>A (ACTR8)
NM_018725.4:c.1254C>T (IL17RB) MANE Select	NP_061195.2:p.Asn418=