Canonical Allele Identifier: CA2456465

Gene: IL17RB ACTR8

Linked Data

• dbSNP Id: rs2232350
• ExAC: 3:53899178 T / C
• gnomAD v2: 3-53899178-T-C
• gnomAD v3: 3-53865151-T-C
• gnomAD v4: 3-53865151-T-C
• COSMIC: COSM149404
• MyVariant Identifiers: chr3:g.53899178T>C (hg19) ; chr3:g.53865151T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53865151T>C , CM000665.2:g.53865151T>C	GRCh38
NC_000003.11:g.53899178T>C , CM000665.1:g.53899178T>C	GRCh37
NC_000003.10:g.53874218T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000288167.8:c.1352T>C (IL17RB) MANE Select	ENSP00000288167.3:p.Ile451Thr
ENST00000288167.7:c.1352T>C (IL17RB)	ENSP00000288167.3:p.Ile451Thr
ENST00000475124.1:n.2385T>C (IL17RB)
NM_018725.3:c.1352T>C (IL17RB)	NP_061195.2:p.Ile451Thr
XM_005265310.3:c.1439T>C (IL17RB)	XP_005265367.1:p.Ile480Thr
XM_005265311.3:c.1391T>C (IL17RB)	XP_005265368.1:p.Ile464Thr
XM_005265312.3:c.1304T>C (IL17RB)	XP_005265369.1:p.Ile435Thr
XM_005265587.3:c.*46-132A>G (ACTR8)	XP_005265644.1:n.*46-132A>G
XM_011533940.1:c.1088T>C (IL17RB)	XP_011532242.1:p.Ile363Thr
XR_245147.3:n.1653T>C (IL17RB)
XR_940467.1:n.1518T>C (IL17RB)
XR_940468.1:n.1431T>C (IL17RB)
XM_005265310.5:c.1439T>C (IL17RB)	XP_005265367.1:p.Ile480Thr
XM_005265311.5:c.1391T>C (IL17RB)	XP_005265368.1:p.Ile464Thr
XM_005265312.5:c.1304T>C (IL17RB)	XP_005265369.1:p.Ile435Thr
XM_005265587.5:c.*46-132A>G (ACTR8)	XP_005265644.1:n.*46-132A>G
XM_011533941.3:c.*232T>C (IL17RB)	XP_011532243.1:n.*232T>C
XM_011534249.3:c.*3568A>G (ACTR8)	XP_011532551.1:n.*3568A>G
XM_017006804.2:c.1088T>C (IL17RB)	XP_016862293.1:p.Ile363Thr
XM_017006805.2:c.1040T>C (IL17RB)	XP_016862294.1:p.Ile347Thr
XM_017006806.2:c.1001T>C (IL17RB)	XP_016862295.1:p.Ile334Thr
XM_017006807.2:c.*232T>C (IL17RB)	XP_016862296.1:n.*232T>C
XR_940516.3:n.5521A>G (ACTR8)
NM_018725.4:c.1352T>C (IL17RB) MANE Select	NP_061195.2:p.Ile451Thr