Canonical Allele Identifier: CA364435169
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs1421825821
gnomAD v3: 6-52186447-A-T
gnomAD v4: 6-52186447-A-T
MyVariant Identifiers: chr6:g.52051245A>T (hg19) chr6:g.52186447A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186447A>T , CM000668.2:g.52186447A>T GRCh38
NC_000006.11:g.52051245A>T , CM000668.1:g.52051245A>T GRCh37
NC_000006.10:g.52159204A>T NCBI36
NG_033021.1:g.5061A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.16A>T MANE Select ENSP00000497968.1:p.Thr6Ser
ENST00000340057.1:c.16A>T ENSP00000344192.1:p.Thr6Ser
NM_002190.2:c.16A>T NP_002181.1:p.Thr6Ser
NM_002190.3:c.16A>T MANE Select NP_002181.1:p.Thr6Ser
Search 100 bp 5'
Search 100 bp 3'