Canonical Allele Identifier: CA353248919

Gene: IL17RB ACTR8

Linked Data

• MyVariant Identifiers: chr3:g.53899180G>C (hg19) ; chr3:g.53865153G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53865153G>C , CM000665.2:g.53865153G>C	GRCh38
NC_000003.11:g.53899180G>C , CM000665.1:g.53899180G>C	GRCh37
NC_000003.10:g.53874220G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000288167.8:c.1354G>C (IL17RB) MANE Select	ENSP00000288167.3:p.Asp452His
ENST00000288167.7:c.1354G>C (IL17RB)	ENSP00000288167.3:p.Asp452His
ENST00000475124.1:n.2387G>C (IL17RB)
NM_018725.3:c.1354G>C (IL17RB)	NP_061195.2:p.Asp452His
XM_005265310.3:c.1441G>C (IL17RB)	XP_005265367.1:p.Asp481His
XM_005265311.3:c.1393G>C (IL17RB)	XP_005265368.1:p.Asp465His
XM_005265312.3:c.1306G>C (IL17RB)	XP_005265369.1:p.Asp436His
XM_005265587.3:c.*46-134C>G (ACTR8)	XP_005265644.1:n.*46-134C>G
XM_011533940.1:c.1090G>C (IL17RB)	XP_011532242.1:p.Asp364His
XR_245147.3:n.1655G>C (IL17RB)
XR_940467.1:n.1520G>C (IL17RB)
XR_940468.1:n.1433G>C (IL17RB)
XM_005265310.5:c.1441G>C (IL17RB)	XP_005265367.1:p.Asp481His
XM_005265311.5:c.1393G>C (IL17RB)	XP_005265368.1:p.Asp465His
XM_005265312.5:c.1306G>C (IL17RB)	XP_005265369.1:p.Asp436His
XM_005265587.5:c.*46-134C>G (ACTR8)	XP_005265644.1:n.*46-134C>G
XM_011533941.3:c.*234G>C (IL17RB)	XP_011532243.1:n.*234G>C
XM_011534249.3:c.*3566C>G (ACTR8)	XP_011532551.1:n.*3566C>G
XM_017006804.2:c.1090G>C (IL17RB)	XP_016862293.1:p.Asp364His
XM_017006805.2:c.1042G>C (IL17RB)	XP_016862294.1:p.Asp348His
XM_017006806.2:c.1003G>C (IL17RB)	XP_016862295.1:p.Asp335His
XM_017006807.2:c.*234G>C (IL17RB)	XP_016862296.1:n.*234G>C
XR_940516.3:n.5519C>G (ACTR8)
NM_018725.4:c.1354G>C (IL17RB) MANE Select	NP_061195.2:p.Asp452His