Canonical Allele Identifier: CA353248971

Gene: IL17RB ACTR8

Linked Data

• dbSNP Id: rs778086828
• gnomAD v2: 3-53899192-G-C
• gnomAD v4: 3-53865165-G-C
• MyVariant Identifiers: chr3:g.53899192G>C (hg19) ; chr3:g.53865165G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53865165G>C , CM000665.2:g.53865165G>C	GRCh38
NC_000003.11:g.53899192G>C , CM000665.1:g.53899192G>C	GRCh37
NC_000003.10:g.53874232G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288167.8:c.1366G>C (IL17RB) MANE Select	ENSP00000288167.3:p.Asp456His
ENST00000288167.7:c.1366G>C (IL17RB)	ENSP00000288167.3:p.Asp456His
ENST00000475124.1:n.2399G>C (IL17RB)
NM_018725.3:c.1366G>C (IL17RB)	NP_061195.2:p.Asp456His
XM_005265310.3:c.1453G>C (IL17RB)	XP_005265367.1:p.Asp485His
XM_005265311.3:c.1405G>C (IL17RB)	XP_005265368.1:p.Asp469His
XM_005265312.3:c.1318G>C (IL17RB)	XP_005265369.1:p.Asp440His
XM_005265587.3:c.*46-146C>G (ACTR8)	XP_005265644.1:n.*46-146C>G
XM_011533940.1:c.1102G>C (IL17RB)	XP_011532242.1:p.Asp368His
XR_245147.3:n.1667G>C (IL17RB)
XR_940467.1:n.1532G>C (IL17RB)
XR_940468.1:n.1445G>C (IL17RB)
XM_005265310.5:c.1453G>C (IL17RB)	XP_005265367.1:p.Asp485His
XM_005265311.5:c.1405G>C (IL17RB)	XP_005265368.1:p.Asp469His
XM_005265312.5:c.1318G>C (IL17RB)	XP_005265369.1:p.Asp440His
XM_005265587.5:c.*46-146C>G (ACTR8)	XP_005265644.1:n.*46-146C>G
XM_011533941.3:c.*246G>C (IL17RB)	XP_011532243.1:n.*246G>C
XM_011534249.3:c.*3554C>G (ACTR8)	XP_011532551.1:n.*3554C>G
XM_017006804.2:c.1102G>C (IL17RB)	XP_016862293.1:p.Asp368His
XM_017006805.2:c.1054G>C (IL17RB)	XP_016862294.1:p.Asp352His
XM_017006806.2:c.1015G>C (IL17RB)	XP_016862295.1:p.Asp339His
XM_017006807.2:c.*246G>C (IL17RB)	XP_016862296.1:n.*246G>C
XR_940516.3:n.5507C>G (ACTR8)
NM_018725.4:c.1366G>C (IL17RB) MANE Select	NP_061195.2:p.Asp456His