Canonical Allele Identifier: CA433896810
Gene: IL17RB HGNC NCBI
ACTR8 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.53899176G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53865149G>A , CM000665.2:g.53865149G>A GRCh38
NC_000003.11:g.53899176G>A , CM000665.1:g.53899176G>A GRCh37
NC_000003.10:g.53874216G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000288167.8:c.1350G>A (IL17RB) MANE Select ENSP00000288167.3:p.Glu450=
ENST00000288167.7:c.1350G>A (IL17RB) ENSP00000288167.3:p.Glu450=
ENST00000475124.1:n.2383G>A (IL17RB)
NM_018725.3:c.1350G>A (IL17RB) NP_061195.2:p.Glu450=
XM_005265310.3:c.1437G>A (IL17RB) XP_005265367.1:p.Glu479=
XM_005265311.3:c.1389G>A (IL17RB) XP_005265368.1:p.Glu463=
XM_005265312.3:c.1302G>A (IL17RB) XP_005265369.1:p.Glu434=
XM_005265587.3:c.*46-130C>T (ACTR8) XP_005265644.1:n.*46-130C>T
XM_011533940.1:c.1086G>A (IL17RB) XP_011532242.1:p.Glu362=
XR_245147.3:n.1651G>A (IL17RB)
XR_940467.1:n.1516G>A (IL17RB)
XR_940468.1:n.1429G>A (IL17RB)
XM_005265310.5:c.1437G>A (IL17RB) XP_005265367.1:p.Glu479=
XM_005265311.5:c.1389G>A (IL17RB) XP_005265368.1:p.Glu463=
XM_005265312.5:c.1302G>A (IL17RB) XP_005265369.1:p.Glu434=
XM_005265587.5:c.*46-130C>T (ACTR8) XP_005265644.1:n.*46-130C>T
XM_011533941.3:c.*230G>A (IL17RB) XP_011532243.1:n.*230G>A
XM_011534249.3:c.*3570C>T (ACTR8) XP_011532551.1:n.*3570C>T
XM_017006804.2:c.1086G>A (IL17RB) XP_016862293.1:p.Glu362=
XM_017006805.2:c.1038G>A (IL17RB) XP_016862294.1:p.Glu346=
XM_017006806.2:c.999G>A (IL17RB) XP_016862295.1:p.Glu333=
XM_017006807.2:c.*230G>A (IL17RB) XP_016862296.1:n.*230G>A
XR_940516.3:n.5523C>T (ACTR8)
NM_018725.4:c.1350G>A (IL17RB) MANE Select NP_061195.2:p.Glu450=