Canonical Allele Identifier: CA353248620

Gene: IL17RB ACTR8

Linked Data

• MyVariant Identifiers: chr3:g.53899099C>T (hg19) ; chr3:g.53865072C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53865072C>T , CM000665.2:g.53865072C>T	GRCh38
NC_000003.11:g.53899099C>T , CM000665.1:g.53899099C>T	GRCh37
NC_000003.10:g.53874139C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288167.8:c.1273C>T (IL17RB) MANE Select	ENSP00000288167.3:p.Leu425Phe
ENST00000288167.7:c.1273C>T (IL17RB)	ENSP00000288167.3:p.Leu425Phe
ENST00000475124.1:n.2306C>T (IL17RB)
NM_018725.3:c.1273C>T (IL17RB)	NP_061195.2:p.Leu425Phe
XM_005265310.3:c.1360C>T (IL17RB)	XP_005265367.1:p.Leu454Phe
XM_005265311.3:c.1312C>T (IL17RB)	XP_005265368.1:p.Leu438Phe
XM_005265312.3:c.1225C>T (IL17RB)	XP_005265369.1:p.Leu409Phe
XM_005265587.3:c.*46-53G>A (ACTR8)	XP_005265644.1:n.*46-53G>A
XM_011533940.1:c.1009C>T (IL17RB)	XP_011532242.1:p.Leu337Phe
XR_245147.3:n.1574C>T (IL17RB)
XR_940467.1:n.1439C>T (IL17RB)
XR_940468.1:n.1352C>T (IL17RB)
XM_005265310.5:c.1360C>T (IL17RB)	XP_005265367.1:p.Leu454Phe
XM_005265311.5:c.1312C>T (IL17RB)	XP_005265368.1:p.Leu438Phe
XM_005265312.5:c.1225C>T (IL17RB)	XP_005265369.1:p.Leu409Phe
XM_005265587.5:c.*46-53G>A (ACTR8)	XP_005265644.1:n.*46-53G>A
XM_011533941.3:c.*153C>T (IL17RB)	XP_011532243.1:n.*153C>T
XM_011534249.3:c.*3647G>A (ACTR8)	XP_011532551.1:n.*3647G>A
XM_017006804.2:c.1009C>T (IL17RB)	XP_016862293.1:p.Leu337Phe
XM_017006805.2:c.961C>T (IL17RB)	XP_016862294.1:p.Leu321Phe
XM_017006806.2:c.922C>T (IL17RB)	XP_016862295.1:p.Leu308Phe
XM_017006807.2:c.*153C>T (IL17RB)	XP_016862296.1:n.*153C>T
XR_940516.3:n.5600G>A (ACTR8)
NM_018725.4:c.1273C>T (IL17RB) MANE Select	NP_061195.2:p.Leu425Phe