Canonical Allele Identifier: CA1023900127
Gene: IL17RA HGNC NCBI

Linked Data

dbSNP Id: rs2061319968
gnomAD v3: 22-17084963-G-A
gnomAD v4: 22-17084963-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17084963G>A , CM000684.2:g.17084963G>A GRCh38
NC_000022.10:g.17565853G>A , CM000684.1:g.17565853G>A GRCh37
NC_000022.9:g.15945853G>A NCBI36
NG_028257.1:g.5003G>A , LRG_355:g.5003G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000319363.10:c.-129G>A ENSP00000320936.6:n.-129G>A
ENST00000477874.1:n.10G>A
ENST00000612619.1:c.-129G>A ENSP00000479970.1:n.-129G>A
NM_001289905.1:c.-129G>A NP_001276834.1:n.-129G>A
NM_014339.6:c.-129G>A , LRG_355t1:c.-129G>A NP_055154.3:n.-129G>A
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