Canonical Allele Identifier: CA433896823

Gene: IL17RB ACTR8

Linked Data

• MyVariant Identifiers: chr3:g.53899182T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53865155T>C , CM000665.2:g.53865155T>C	GRCh38
NC_000003.11:g.53899182T>C , CM000665.1:g.53899182T>C	GRCh37
NC_000003.10:g.53874222T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000288167.8:c.1356T>C (IL17RB) MANE Select	ENSP00000288167.3:p.Asp452=
ENST00000288167.7:c.1356T>C (IL17RB)	ENSP00000288167.3:p.Asp452=
ENST00000475124.1:n.2389T>C (IL17RB)
NM_018725.3:c.1356T>C (IL17RB)	NP_061195.2:p.Asp452=
XM_005265310.3:c.1443T>C (IL17RB)	XP_005265367.1:p.Asp481=
XM_005265311.3:c.1395T>C (IL17RB)	XP_005265368.1:p.Asp465=
XM_005265312.3:c.1308T>C (IL17RB)	XP_005265369.1:p.Asp436=
XM_005265587.3:c.*46-136A>G (ACTR8)	XP_005265644.1:n.*46-136A>G
XM_011533940.1:c.1092T>C (IL17RB)	XP_011532242.1:p.Asp364=
XR_245147.3:n.1657T>C (IL17RB)
XR_940467.1:n.1522T>C (IL17RB)
XR_940468.1:n.1435T>C (IL17RB)
XM_005265310.5:c.1443T>C (IL17RB)	XP_005265367.1:p.Asp481=
XM_005265311.5:c.1395T>C (IL17RB)	XP_005265368.1:p.Asp465=
XM_005265312.5:c.1308T>C (IL17RB)	XP_005265369.1:p.Asp436=
XM_005265587.5:c.*46-136A>G (ACTR8)	XP_005265644.1:n.*46-136A>G
XM_011533941.3:c.*236T>C (IL17RB)	XP_011532243.1:n.*236T>C
XM_011534249.3:c.*3564A>G (ACTR8)	XP_011532551.1:n.*3564A>G
XM_017006804.2:c.1092T>C (IL17RB)	XP_016862293.1:p.Asp364=
XM_017006805.2:c.1044T>C (IL17RB)	XP_016862294.1:p.Asp348=
XM_017006806.2:c.1005T>C (IL17RB)	XP_016862295.1:p.Asp335=
XM_017006807.2:c.*236T>C (IL17RB)	XP_016862296.1:n.*236T>C
XR_940516.3:n.5517A>G (ACTR8)
NM_018725.4:c.1356T>C (IL17RB) MANE Select	NP_061195.2:p.Asp452=