Canonical Allele Identifier: CA364435356
Gene: IL17A HGNC NCBI

Linked Data

ClinVar Variation Id: 3109126
ClinVar RCV Id: RCV004404993
dbSNP Id: rs1394860452
gnomAD v2: 6-52051255-T-C
gnomAD v3: 6-52186457-T-C
gnomAD v4: 6-52186457-T-C
MyVariant Identifiers: chr6:g.52051255T>C (hg19) chr6:g.52186457T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186457T>C , CM000668.2:g.52186457T>C GRCh38
NC_000006.11:g.52051255T>C , CM000668.1:g.52051255T>C GRCh37
NC_000006.10:g.52159214T>C NCBI36
NG_033021.1:g.5071T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.26T>C MANE Select ENSP00000497968.1:p.Val9Ala
ENST00000340057.1:c.26T>C ENSP00000344192.1:p.Val9Ala
NM_002190.2:c.26T>C NP_002181.1:p.Val9Ala
NM_002190.3:c.26T>C MANE Select NP_002181.1:p.Val9Ala
Search 100 bp 5'
Search 100 bp 3'