Canonical Allele Identifier: CA567311332
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs1322729755
gnomAD v2: 6-52051267-C-A
gnomAD v4: 6-52186469-C-A
MyVariant Identifiers: chr6:g.52051267C>A (hg19) chr6:g.52186469C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186469C>A , CM000668.2:g.52186469C>A GRCh38
NC_000006.11:g.52051267C>A , CM000668.1:g.52051267C>A GRCh37
NC_000006.10:g.52159226C>A NCBI36
NG_033021.1:g.5083C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.27+11C>A MANE Select ENSP00000497968.1:n.27+11C>A
ENST00000340057.1:c.27+11C>A ENSP00000344192.1:n.27+11C>A
NM_002190.2:c.27+11C>A NP_002181.1:n.27+11C>A
NM_002190.3:c.27+11C>A MANE Select NP_002181.1:n.27+11C>A
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