Canonical Allele Identifier: CA364435188
Gene: IL17A HGNC NCBI

Linked Data

gnomAD v4: 6-52186450-T-A
MyVariant Identifiers: chr6:g.52051248T>A (hg19) chr6:g.52186450T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186450T>A , CM000668.2:g.52186450T>A GRCh38
NC_000006.11:g.52051248T>A , CM000668.1:g.52051248T>A GRCh37
NC_000006.10:g.52159207T>A NCBI36
NG_033021.1:g.5064T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.19T>A MANE Select ENSP00000497968.1:p.Ser7Thr
ENST00000340057.1:c.19T>A ENSP00000344192.1:p.Ser7Thr
NM_002190.2:c.19T>A NP_002181.1:p.Ser7Thr
NM_002190.3:c.19T>A MANE Select NP_002181.1:p.Ser7Thr
Search 100 bp 5'
Search 100 bp 3'