Canonical Allele Identifier: CA1023900148
Gene: IL17RA HGNC NCBI

Linked Data

dbSNP Id: rs2061320093
gnomAD v3: 22-17084986-A-T
gnomAD v4: 22-17084986-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17084986A>T , CM000684.2:g.17084986A>T GRCh38
NC_000022.10:g.17565876A>T , CM000684.1:g.17565876A>T GRCh37
NC_000022.9:g.15945876A>T NCBI36
NG_028257.1:g.5026A>T , LRG_355:g.5026A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000319363.10:c.-106A>T ENSP00000320936.6:n.-106A>T
ENST00000477874.1:n.33A>T
ENST00000612619.1:c.-106A>T ENSP00000479970.1:n.-106A>T
NM_001289905.1:c.-106A>T NP_001276834.1:n.-106A>T
NM_014339.6:c.-106A>T , LRG_355t1:c.-106A>T NP_055154.3:n.-106A>T
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