Canonical Allele Identifier: CA2456446
Gene: IL17RB HGNC NCBI
ACTR8 HGNC NCBI

Linked Data

dbSNP Id: rs753185213
gnomAD v2: 3-53899077-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53865050G>A , CM000665.2:g.53865050G>A GRCh38
NC_000003.11:g.53899077G>A , CM000665.1:g.53899077G>A GRCh37
NC_000003.10:g.53874117G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288167.8:c.1251G>A (IL17RB) MANE Select ENSP00000288167.3:p.Glu417=
ENST00000288167.7:c.1251G>A (IL17RB) ENSP00000288167.3:p.Glu417=
ENST00000475124.1:n.2284G>A (IL17RB)
NM_018725.3:c.1251G>A (IL17RB) NP_061195.2:p.Glu417=
XM_005265310.3:c.1338G>A (IL17RB) XP_005265367.1:p.Glu446=
XM_005265311.3:c.1290G>A (IL17RB) XP_005265368.1:p.Glu430=
XM_005265312.3:c.1203G>A (IL17RB) XP_005265369.1:p.Glu401=
XM_005265587.3:c.*46-31C>T (ACTR8) XP_005265644.1:n.*46-31C>T
XM_011533940.1:c.987G>A (IL17RB) XP_011532242.1:p.Glu329=
XR_245147.3:n.1552G>A (IL17RB)
XR_940467.1:n.1417G>A (IL17RB)
XR_940468.1:n.1330G>A (IL17RB)
XM_005265310.5:c.1338G>A (IL17RB) XP_005265367.1:p.Glu446=
XM_005265311.5:c.1290G>A (IL17RB) XP_005265368.1:p.Glu430=
XM_005265312.5:c.1203G>A (IL17RB) XP_005265369.1:p.Glu401=
XM_005265587.5:c.*46-31C>T (ACTR8) XP_005265644.1:n.*46-31C>T
XM_011533941.3:c.*131G>A (IL17RB) XP_011532243.1:n.*131G>A
XM_011534249.3:c.*3669C>T (ACTR8) XP_011532551.1:n.*3669C>T
XM_017006804.2:c.987G>A (IL17RB) XP_016862293.1:p.Glu329=
XM_017006805.2:c.939G>A (IL17RB) XP_016862294.1:p.Glu313=
XM_017006806.2:c.900G>A (IL17RB) XP_016862295.1:p.Glu300=
XM_017006807.2:c.*131G>A (IL17RB) XP_016862296.1:n.*131G>A
XR_940516.3:n.5622C>T (ACTR8)
NM_018725.4:c.1251G>A (IL17RB) MANE Select NP_061195.2:p.Glu417=