Canonical Allele Identifier: CA321139647
Gene: IL17RA HGNC NCBI

Linked Data

dbSNP Id: rs892085069
gnomAD v3: 22-17084971-T-C
gnomAD v4: 22-17084971-T-C
MyVariant Identifiers: chr22:g.17565861T>C (hg19) chr22:g.17084971T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17084971T>C , CM000684.2:g.17084971T>C GRCh38
NC_000022.10:g.17565861T>C , CM000684.1:g.17565861T>C GRCh37
NC_000022.9:g.15945861T>C NCBI36
NG_028257.1:g.5011T>C , LRG_355:g.5011T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000319363.10:c.-121T>C ENSP00000320936.6:n.-121T>C
ENST00000477874.1:n.18T>C
ENST00000612619.1:c.-121T>C ENSP00000479970.1:n.-121T>C
NM_001289905.1:c.-121T>C NP_001276834.1:n.-121T>C
NM_014339.6:c.-121T>C , LRG_355t1:c.-121T>C NP_055154.3:n.-121T>C
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