Canonical Allele Identifier: CA353248957
Gene: IL17RB HGNC NCBI
ACTR8 HGNC NCBI

Linked Data

dbSNP Id: rs1261554621

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53865162G>A , CM000665.2:g.53865162G>A GRCh38
NC_000003.11:g.53899189G>A , CM000665.1:g.53899189G>A GRCh37
NC_000003.10:g.53874229G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000288167.8:c.1363G>A (IL17RB) MANE Select ENSP00000288167.3:p.Asp455Asn
ENST00000288167.7:c.1363G>A (IL17RB) ENSP00000288167.3:p.Asp455Asn
ENST00000475124.1:n.2396G>A (IL17RB)
NM_018725.3:c.1363G>A (IL17RB) NP_061195.2:p.Asp455Asn
XM_005265310.3:c.1450G>A (IL17RB) XP_005265367.1:p.Asp484Asn
XM_005265311.3:c.1402G>A (IL17RB) XP_005265368.1:p.Asp468Asn
XM_005265312.3:c.1315G>A (IL17RB) XP_005265369.1:p.Asp439Asn
XM_005265587.3:c.*46-143C>T (ACTR8) XP_005265644.1:n.*46-143C>T
XM_011533940.1:c.1099G>A (IL17RB) XP_011532242.1:p.Asp367Asn
XR_245147.3:n.1664G>A (IL17RB)
XR_940467.1:n.1529G>A (IL17RB)
XR_940468.1:n.1442G>A (IL17RB)
XM_005265310.5:c.1450G>A (IL17RB) XP_005265367.1:p.Asp484Asn
XM_005265311.5:c.1402G>A (IL17RB) XP_005265368.1:p.Asp468Asn
XM_005265312.5:c.1315G>A (IL17RB) XP_005265369.1:p.Asp439Asn
XM_005265587.5:c.*46-143C>T (ACTR8) XP_005265644.1:n.*46-143C>T
XM_011533941.3:c.*243G>A (IL17RB) XP_011532243.1:n.*243G>A
XM_011534249.3:c.*3557C>T (ACTR8) XP_011532551.1:n.*3557C>T
XM_017006804.2:c.1099G>A (IL17RB) XP_016862293.1:p.Asp367Asn
XM_017006805.2:c.1051G>A (IL17RB) XP_016862294.1:p.Asp351Asn
XM_017006806.2:c.1012G>A (IL17RB) XP_016862295.1:p.Asp338Asn
XM_017006807.2:c.*243G>A (IL17RB) XP_016862296.1:n.*243G>A
XR_940516.3:n.5510C>T (ACTR8)
NM_018725.4:c.1363G>A (IL17RB) MANE Select NP_061195.2:p.Asp455Asn