Canonical Allele Identifier: CA2456468
Gene: IL17RB HGNC NCBI
ACTR8 HGNC NCBI

Linked Data

dbSNP Id: rs752842028
gnomAD v2: 3-53899184-C-T
gnomAD v4: 3-53865157-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53865157C>T , CM000665.2:g.53865157C>T GRCh38
NC_000003.11:g.53899184C>T , CM000665.1:g.53899184C>T GRCh37
NC_000003.10:g.53874224C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000288167.8:c.1358C>T (IL17RB) MANE Select ENSP00000288167.3:p.Thr453Ile
ENST00000288167.7:c.1358C>T (IL17RB) ENSP00000288167.3:p.Thr453Ile
ENST00000475124.1:n.2391C>T (IL17RB)
NM_018725.3:c.1358C>T (IL17RB) NP_061195.2:p.Thr453Ile
XM_005265310.3:c.1445C>T (IL17RB) XP_005265367.1:p.Thr482Ile
XM_005265311.3:c.1397C>T (IL17RB) XP_005265368.1:p.Thr466Ile
XM_005265312.3:c.1310C>T (IL17RB) XP_005265369.1:p.Thr437Ile
XM_005265587.3:c.*46-138G>A (ACTR8) XP_005265644.1:n.*46-138G>A
XM_011533940.1:c.1094C>T (IL17RB) XP_011532242.1:p.Thr365Ile
XR_245147.3:n.1659C>T (IL17RB)
XR_940467.1:n.1524C>T (IL17RB)
XR_940468.1:n.1437C>T (IL17RB)
XM_005265310.5:c.1445C>T (IL17RB) XP_005265367.1:p.Thr482Ile
XM_005265311.5:c.1397C>T (IL17RB) XP_005265368.1:p.Thr466Ile
XM_005265312.5:c.1310C>T (IL17RB) XP_005265369.1:p.Thr437Ile
XM_005265587.5:c.*46-138G>A (ACTR8) XP_005265644.1:n.*46-138G>A
XM_011533941.3:c.*238C>T (IL17RB) XP_011532243.1:n.*238C>T
XM_011534249.3:c.*3562G>A (ACTR8) XP_011532551.1:n.*3562G>A
XM_017006804.2:c.1094C>T (IL17RB) XP_016862293.1:p.Thr365Ile
XM_017006805.2:c.1046C>T (IL17RB) XP_016862294.1:p.Thr349Ile
XM_017006806.2:c.1007C>T (IL17RB) XP_016862295.1:p.Thr336Ile
XM_017006807.2:c.*238C>T (IL17RB) XP_016862296.1:n.*238C>T
XR_940516.3:n.5515G>A (ACTR8)
NM_018725.4:c.1358C>T (IL17RB) MANE Select NP_061195.2:p.Thr453Ile