Canonical Allele Identifier: CA638274285
Gene: IL17RA HGNC NCBI

Linked Data

dbSNP Id: rs1346803126
gnomAD v2: 22-17565875-G-C
gnomAD v3: 22-17084985-G-C
gnomAD v4: 22-17084985-G-C
MyVariant Identifiers: chr22:g.17565875G>C (hg19) chr22:g.17084985G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17084985G>C , CM000684.2:g.17084985G>C GRCh38
NC_000022.10:g.17565875G>C , CM000684.1:g.17565875G>C GRCh37
NC_000022.9:g.15945875G>C NCBI36
NG_028257.1:g.5025G>C , LRG_355:g.5025G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000319363.10:c.-107G>C ENSP00000320936.6:n.-107G>C
ENST00000477874.1:n.32G>C
ENST00000612619.1:c.-107G>C ENSP00000479970.1:n.-107G>C
NM_001289905.1:c.-107G>C NP_001276834.1:n.-107G>C
NM_014339.6:c.-107G>C , LRG_355t1:c.-107G>C NP_055154.3:n.-107G>C
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