Canonical Allele Identifier: CA3854196
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs748539355
ExAC: 6:52051288 C / T
gnomAD v2: 6-52051288-C-T
gnomAD v4: 6-52186490-C-T
MyVariant Identifiers: chr6:g.52051288C>T (hg19) chr6:g.52186490C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186490C>T , CM000668.2:g.52186490C>T GRCh38
NC_000006.11:g.52051288C>T , CM000668.1:g.52051288C>T GRCh37
NC_000006.10:g.52159247C>T NCBI36
NG_033021.1:g.5104C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.27+32C>T MANE Select ENSP00000497968.1:n.27+32C>T
ENST00000340057.1:c.27+32C>T ENSP00000344192.1:n.27+32C>T
NM_002190.2:c.27+32C>T NP_002181.1:n.27+32C>T
NM_002190.3:c.27+32C>T MANE Select NP_002181.1:n.27+32C>T
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