Canonical Allele Identifier: CA321139623
Gene: IL17RA HGNC NCBI

Linked Data

dbSNP Id: rs564384700
gnomAD v2: 22-17565846-C-T
gnomAD v3: 22-17084956-C-T
gnomAD v4: 22-17084956-C-T
MyVariant Identifiers: chr22:g.17565846C>T (hg19) chr22:g.17084956C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17084956C>T , CM000684.2:g.17084956C>T GRCh38
NC_000022.10:g.17565846C>T , CM000684.1:g.17565846C>T GRCh37
NC_000022.9:g.15945846C>T NCBI36
NG_028257.1:g.4996C>T , LRG_355:g.4996C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000477874.1:n.3C>T
Search 100 bp 5'
Search 100 bp 3'