Canonical Allele Identifier: CA3854199
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs749745973
ExAC: 6:52051301 G / C
gnomAD v2: 6-52051301-G-C
gnomAD v4: 6-52186503-G-C
MyVariant Identifiers: chr6:g.52051301G>C (hg19) chr6:g.52186503G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186503G>C , CM000668.2:g.52186503G>C GRCh38
NC_000006.11:g.52051301G>C , CM000668.1:g.52051301G>C GRCh37
NC_000006.10:g.52159260G>C NCBI36
NG_033021.1:g.5117G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.27+45G>C MANE Select ENSP00000497968.1:n.27+45G>C
ENST00000340057.1:c.27+45G>C ENSP00000344192.1:n.27+45G>C
NM_002190.2:c.27+45G>C NP_002181.1:n.27+45G>C
NM_002190.3:c.27+45G>C MANE Select NP_002181.1:n.27+45G>C
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