Canonical Allele Identifier: CA2456484
Gene: IL17RB HGNC NCBI
ACTR8 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1043261

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53865249C>T , CM000665.2:g.53865249C>T GRCh38
NC_000003.10:g.53874316C>T NCBI36
NC_000003.11:g.53899276C>T , CM000665.1:g.53899276C>T GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000288167.7:c.1450C>T ENSP00000288167.3:p.Gln484Ter
ENST00000475124.1:n.2483C>T
NM_018725.3:c.1450C>T (IL17RB) VV NP_061195.2:p.Gln484Ter
XM_005265310.3:c.1537C>T (IL17RB) XP_005265367.1:p.Gln513Ter
XM_005265311.3:c.1489C>T (IL17RB) XP_005265368.1:p.Gln497Ter
XM_005265312.3:c.1402C>T (IL17RB) XP_005265369.1:p.Gln468Ter
XM_005265587.3:c.*46-230G>A (ACTR8) XP_005265644.1:p.=
XM_011533940.1:c.1186C>T (IL17RB) XP_011532242.1:p.Gln396Ter
XR_245147.3:n.1751C>T (IL17RB)
XR_940467.1:n.1616C>T (IL17RB)
XR_940468.1:n.1529C>T (IL17RB)