Canonical Allele Identifier: CA567311330
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs1226942213
gnomAD v2: 6-52051263-C-G
gnomAD v4: 6-52186465-C-G
MyVariant Identifiers: chr6:g.52051263C>G (hg19) chr6:g.52186465C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186465C>G , CM000668.2:g.52186465C>G GRCh38
NC_000006.11:g.52051263C>G , CM000668.1:g.52051263C>G GRCh37
NC_000006.10:g.52159222C>G NCBI36
NG_033021.1:g.5079C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.27+7C>G MANE Select ENSP00000497968.1:n.27+7C>G
ENST00000340057.1:c.27+7C>G ENSP00000344192.1:n.27+7C>G
NM_002190.2:c.27+7C>G NP_002181.1:n.27+7C>G
NM_002190.3:c.27+7C>G MANE Select NP_002181.1:n.27+7C>G
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