Canonical Allele Identifier: CA1365506996

Gene: IL17RB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53849695C= , CM000665.2:g.53849695C=	GRCh38
NC_000003.11:g.53883722C= , CM000665.1:g.53883722C=	GRCh37
NC_000003.10:g.53858762C=	NCBI36
NG_028042.1:g.1699G=

Transcript Alleles

HGVS	Amino-acid Change
NM_018725.4:c.126C= MANE Select	NP_061195.2:p.Pro42=
ENST00000288167.8:c.126C= MANE Select	ENSP00000288167.3:p.Pro42=
NM_018725.3:c.126C=	NP_061195.2:p.Pro42=
ENST00000288167.7:c.126C=	ENSP00000288167.3:p.Pro42=
ENST00000475124.1:n.131C=
ENST00000494338.1:c.126C=	ENSP00000418638.1:p.Pro42=
XM_005265310.3:c.126C=	XP_005265367.1:p.Pro42=
XM_005265310.5:c.126C=	XP_005265367.1:p.Pro42=
XM_005265311.3:c.126C=	XP_005265368.1:p.Pro42=
XM_005265311.5:c.126C=	XP_005265368.1:p.Pro42=
XM_005265312.3:c.126C=	XP_005265369.1:p.Pro42=
XM_005265312.5:c.126C=	XP_005265369.1:p.Pro42=
XM_011533941.1:c.126C=	XP_011532243.1:p.Pro42=
XM_011533941.3:c.126C=	XP_011532243.1:p.Pro42=
XM_017006804.2:c.-98C=	XP_016862293.1:n.-98C=
XM_017006805.2:c.-98C=	XP_016862294.1:n.-98C=
XM_017006806.2:c.-98C=	XP_016862295.1:n.-98C=
XM_017006807.2:c.126C=	XP_016862296.1:p.Pro42=
XM_024453634.1:c.126C=	XP_024309402.1:p.Pro42=
XM_024453635.1:c.126C=	XP_024309403.1:p.Pro42=
XM_024453636.1:c.126C=	XP_024309404.1:p.Pro42=
XR_245147.3:n.165C=
XR_940467.1:n.165C=
XR_940468.1:n.165C=