Canonical Allele Identifier: CA353249083

Gene: IL17RB ACTR8

Linked Data

• MyVariant Identifiers: chr3:g.53899222T>G (hg19) ; chr3:g.53865195T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53865195T>G , CM000665.2:g.53865195T>G	GRCh38
NC_000003.11:g.53899222T>G , CM000665.1:g.53899222T>G	GRCh37
NC_000003.10:g.53874262T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288167.8:c.1396T>G (IL17RB) MANE Select	ENSP00000288167.3:p.Tyr466Asp
ENST00000288167.7:c.1396T>G (IL17RB)	ENSP00000288167.3:p.Tyr466Asp
ENST00000475124.1:n.2429T>G (IL17RB)
NM_018725.3:c.1396T>G (IL17RB)	NP_061195.2:p.Tyr466Asp
XM_005265310.3:c.1483T>G (IL17RB)	XP_005265367.1:p.Tyr495Asp
XM_005265311.3:c.1435T>G (IL17RB)	XP_005265368.1:p.Tyr479Asp
XM_005265312.3:c.1348T>G (IL17RB)	XP_005265369.1:p.Tyr450Asp
XM_005265587.3:c.*46-176A>C (ACTR8)	XP_005265644.1:n.*46-176A>C
XM_011533940.1:c.1132T>G (IL17RB)	XP_011532242.1:p.Tyr378Asp
XR_245147.3:n.1697T>G (IL17RB)
XR_940467.1:n.1562T>G (IL17RB)
XR_940468.1:n.1475T>G (IL17RB)
XM_005265310.5:c.1483T>G (IL17RB)	XP_005265367.1:p.Tyr495Asp
XM_005265311.5:c.1435T>G (IL17RB)	XP_005265368.1:p.Tyr479Asp
XM_005265312.5:c.1348T>G (IL17RB)	XP_005265369.1:p.Tyr450Asp
XM_005265587.5:c.*46-176A>C (ACTR8)	XP_005265644.1:n.*46-176A>C
XM_011533941.3:c.*276T>G (IL17RB)	XP_011532243.1:n.*276T>G
XM_011534249.3:c.*3524A>C (ACTR8)	XP_011532551.1:n.*3524A>C
XM_017006804.2:c.1132T>G (IL17RB)	XP_016862293.1:p.Tyr378Asp
XM_017006805.2:c.1084T>G (IL17RB)	XP_016862294.1:p.Tyr362Asp
XM_017006806.2:c.1045T>G (IL17RB)	XP_016862295.1:p.Tyr349Asp
XM_017006807.2:c.*276T>G (IL17RB)	XP_016862296.1:n.*276T>G
XR_940516.3:n.5477A>C (ACTR8)
NM_018725.4:c.1396T>G (IL17RB) MANE Select	NP_061195.2:p.Tyr466Asp