Canonical Allele Identifier: CA433897109

Gene: IL17RB ACTR8

Linked Data

• MyVariant Identifiers: chr3:g.53899266C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53865239C>T , CM000665.2:g.53865239C>T	GRCh38
NC_000003.11:g.53899266C>T , CM000665.1:g.53899266C>T	GRCh37
NC_000003.10:g.53874306C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288167.8:c.1440C>T (IL17RB) MANE Select	ENSP00000288167.3:p.Leu480=
ENST00000288167.7:c.1440C>T (IL17RB)	ENSP00000288167.3:p.Leu480=
ENST00000475124.1:n.2473C>T (IL17RB)
NM_018725.3:c.1440C>T (IL17RB)	NP_061195.2:p.Leu480=
XM_005265310.3:c.1527C>T (IL17RB)	XP_005265367.1:p.Leu509=
XM_005265311.3:c.1479C>T (IL17RB)	XP_005265368.1:p.Leu493=
XM_005265312.3:c.1392C>T (IL17RB)	XP_005265369.1:p.Leu464=
XM_005265587.3:c.*46-220G>A (ACTR8)	XP_005265644.1:n.*46-220G>A
XM_011533940.1:c.1176C>T (IL17RB)	XP_011532242.1:p.Leu392=
XR_245147.3:n.1741C>T (IL17RB)
XR_940467.1:n.1606C>T (IL17RB)
XR_940468.1:n.1519C>T (IL17RB)
XM_005265310.5:c.1527C>T (IL17RB)	XP_005265367.1:p.Leu509=
XM_005265311.5:c.1479C>T (IL17RB)	XP_005265368.1:p.Leu493=
XM_005265312.5:c.1392C>T (IL17RB)	XP_005265369.1:p.Leu464=
XM_005265587.5:c.*46-220G>A (ACTR8)	XP_005265644.1:n.*46-220G>A
XM_011533941.3:c.*320C>T (IL17RB)	XP_011532243.1:n.*320C>T
XM_011534249.3:c.*3480G>A (ACTR8)	XP_011532551.1:n.*3480G>A
XM_017006804.2:c.1176C>T (IL17RB)	XP_016862293.1:p.Leu392=
XM_017006805.2:c.1128C>T (IL17RB)	XP_016862294.1:p.Leu376=
XM_017006806.2:c.1089C>T (IL17RB)	XP_016862295.1:p.Leu363=
XM_017006807.2:c.*320C>T (IL17RB)	XP_016862296.1:n.*320C>T
XR_940516.3:n.5433G>A (ACTR8)
NM_018725.4:c.1440C>T (IL17RB) MANE Select	NP_061195.2:p.Leu480=