Canonical Allele Identifier: CA353248991
Gene: IL17RB HGNC NCBI
ACTR8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53865170C>A , CM000665.2:g.53865170C>A GRCh38
NC_000003.11:g.53899197C>A , CM000665.1:g.53899197C>A GRCh37
NC_000003.10:g.53874237C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288167.8:c.1371C>A (IL17RB) MANE Select ENSP00000288167.3:p.Tyr457Ter
ENST00000288167.7:c.1371C>A (IL17RB) ENSP00000288167.3:p.Tyr457Ter
ENST00000475124.1:n.2404C>A (IL17RB)
NM_018725.3:c.1371C>A (IL17RB) NP_061195.2:p.Tyr457Ter
XM_005265310.3:c.1458C>A (IL17RB) XP_005265367.1:p.Tyr486Ter
XM_005265311.3:c.1410C>A (IL17RB) XP_005265368.1:p.Tyr470Ter
XM_005265312.3:c.1323C>A (IL17RB) XP_005265369.1:p.Tyr441Ter
XM_005265587.3:c.*46-151G>T (ACTR8) XP_005265644.1:n.*46-151G>T
XM_011533940.1:c.1107C>A (IL17RB) XP_011532242.1:p.Tyr369Ter
XR_245147.3:n.1672C>A (IL17RB)
XR_940467.1:n.1537C>A (IL17RB)
XR_940468.1:n.1450C>A (IL17RB)
XM_005265310.5:c.1458C>A (IL17RB) XP_005265367.1:p.Tyr486Ter
XM_005265311.5:c.1410C>A (IL17RB) XP_005265368.1:p.Tyr470Ter
XM_005265312.5:c.1323C>A (IL17RB) XP_005265369.1:p.Tyr441Ter
XM_005265587.5:c.*46-151G>T (ACTR8) XP_005265644.1:n.*46-151G>T
XM_011533941.3:c.*251C>A (IL17RB) XP_011532243.1:n.*251C>A
XM_011534249.3:c.*3549G>T (ACTR8) XP_011532551.1:n.*3549G>T
XM_017006804.2:c.1107C>A (IL17RB) XP_016862293.1:p.Tyr369Ter
XM_017006805.2:c.1059C>A (IL17RB) XP_016862294.1:p.Tyr353Ter
XM_017006806.2:c.1020C>A (IL17RB) XP_016862295.1:p.Tyr340Ter
XM_017006807.2:c.*251C>A (IL17RB) XP_016862296.1:n.*251C>A
XR_940516.3:n.5502G>T (ACTR8)
NM_018725.4:c.1371C>A (IL17RB) MANE Select NP_061195.2:p.Tyr457Ter