Canonical Allele Identifier: CA433896718

Gene: IL17RB ACTR8

Linked Data

• MyVariant Identifiers: chr3:g.53899137G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53865110G>A , CM000665.2:g.53865110G>A	GRCh38
NC_000003.11:g.53899137G>A , CM000665.1:g.53899137G>A	GRCh37
NC_000003.10:g.53874177G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288167.8:c.1311G>A (IL17RB) MANE Select	ENSP00000288167.3:p.Gln437=
ENST00000288167.7:c.1311G>A (IL17RB)	ENSP00000288167.3:p.Gln437=
ENST00000475124.1:n.2344G>A (IL17RB)
NM_018725.3:c.1311G>A (IL17RB)	NP_061195.2:p.Gln437=
XM_005265310.3:c.1398G>A (IL17RB)	XP_005265367.1:p.Gln466=
XM_005265311.3:c.1350G>A (IL17RB)	XP_005265368.1:p.Gln450=
XM_005265312.3:c.1263G>A (IL17RB)	XP_005265369.1:p.Gln421=
XM_005265587.3:c.*46-91C>T (ACTR8)	XP_005265644.1:n.*46-91C>T
XM_011533940.1:c.1047G>A (IL17RB)	XP_011532242.1:p.Gln349=
XR_245147.3:n.1612G>A (IL17RB)
XR_940467.1:n.1477G>A (IL17RB)
XR_940468.1:n.1390G>A (IL17RB)
XM_005265310.5:c.1398G>A (IL17RB)	XP_005265367.1:p.Gln466=
XM_005265311.5:c.1350G>A (IL17RB)	XP_005265368.1:p.Gln450=
XM_005265312.5:c.1263G>A (IL17RB)	XP_005265369.1:p.Gln421=
XM_005265587.5:c.*46-91C>T (ACTR8)	XP_005265644.1:n.*46-91C>T
XM_011533941.3:c.*191G>A (IL17RB)	XP_011532243.1:n.*191G>A
XM_011534249.3:c.*3609C>T (ACTR8)	XP_011532551.1:n.*3609C>T
XM_017006804.2:c.1047G>A (IL17RB)	XP_016862293.1:p.Gln349=
XM_017006805.2:c.999G>A (IL17RB)	XP_016862294.1:p.Gln333=
XM_017006806.2:c.960G>A (IL17RB)	XP_016862295.1:p.Gln320=
XM_017006807.2:c.*191G>A (IL17RB)	XP_016862296.1:n.*191G>A
XR_940516.3:n.5562C>T (ACTR8)
NM_018725.4:c.1311G>A (IL17RB) MANE Select	NP_061195.2:p.Gln437=