Canonical Allele Identifier: CA138929659
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs972870076
gnomAD v3: 6-52186526-A-G
gnomAD v4: 6-52186526-A-G
MyVariant Identifiers: chr6:g.52051324A>G (hg19) chr6:g.52186526A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186526A>G , CM000668.2:g.52186526A>G GRCh38
NC_000006.11:g.52051324A>G , CM000668.1:g.52051324A>G GRCh37
NC_000006.10:g.52159283A>G NCBI36
NG_033021.1:g.5140A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.27+68A>G MANE Select ENSP00000497968.1:n.27+68A>G
ENST00000340057.1:c.27+68A>G ENSP00000344192.1:n.27+68A>G
NM_002190.2:c.27+68A>G NP_002181.1:n.27+68A>G
NM_002190.3:c.27+68A>G MANE Select NP_002181.1:n.27+68A>G
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