Canonical Allele Identifier: CA353248540
Gene: IL17RB HGNC NCBI
ACTR8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53865052A>C , CM000665.2:g.53865052A>C GRCh38
NC_000003.11:g.53899079A>C , CM000665.1:g.53899079A>C GRCh37
NC_000003.10:g.53874119A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288167.8:c.1253A>C (IL17RB) MANE Select ENSP00000288167.3:p.Asn418Thr
ENST00000288167.7:c.1253A>C (IL17RB) ENSP00000288167.3:p.Asn418Thr
ENST00000475124.1:n.2286A>C (IL17RB)
NM_018725.3:c.1253A>C (IL17RB) NP_061195.2:p.Asn418Thr
XM_005265310.3:c.1340A>C (IL17RB) XP_005265367.1:p.Asn447Thr
XM_005265311.3:c.1292A>C (IL17RB) XP_005265368.1:p.Asn431Thr
XM_005265312.3:c.1205A>C (IL17RB) XP_005265369.1:p.Asn402Thr
XM_005265587.3:c.*46-33T>G (ACTR8) XP_005265644.1:n.*46-33T>G
XM_011533940.1:c.989A>C (IL17RB) XP_011532242.1:p.Asn330Thr
XR_245147.3:n.1554A>C (IL17RB)
XR_940467.1:n.1419A>C (IL17RB)
XR_940468.1:n.1332A>C (IL17RB)
XM_005265310.5:c.1340A>C (IL17RB) XP_005265367.1:p.Asn447Thr
XM_005265311.5:c.1292A>C (IL17RB) XP_005265368.1:p.Asn431Thr
XM_005265312.5:c.1205A>C (IL17RB) XP_005265369.1:p.Asn402Thr
XM_005265587.5:c.*46-33T>G (ACTR8) XP_005265644.1:n.*46-33T>G
XM_011533941.3:c.*133A>C (IL17RB) XP_011532243.1:n.*133A>C
XM_011534249.3:c.*3667T>G (ACTR8) XP_011532551.1:n.*3667T>G
XM_017006804.2:c.989A>C (IL17RB) XP_016862293.1:p.Asn330Thr
XM_017006805.2:c.941A>C (IL17RB) XP_016862294.1:p.Asn314Thr
XM_017006806.2:c.902A>C (IL17RB) XP_016862295.1:p.Asn301Thr
XM_017006807.2:c.*133A>C (IL17RB) XP_016862296.1:n.*133A>C
XR_940516.3:n.5620T>G (ACTR8)
NM_018725.4:c.1253A>C (IL17RB) MANE Select NP_061195.2:p.Asn418Thr