Canonical Allele Identifier: CA825772120
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs1271251112
gnomAD v3: 6-52186535-T-A
gnomAD v4: 6-52186535-T-A
MyVariant Identifiers: chr6:g.52051333T>A (hg19) chr6:g.52186535T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186535T>A , CM000668.2:g.52186535T>A GRCh38
NC_000006.11:g.52051333T>A , CM000668.1:g.52051333T>A GRCh37
NC_000006.10:g.52159292T>A NCBI36
NG_033021.1:g.5149T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.27+77T>A MANE Select ENSP00000497968.1:n.27+77T>A
ENST00000340057.1:c.27+77T>A ENSP00000344192.1:n.27+77T>A
NM_002190.2:c.27+77T>A NP_002181.1:n.27+77T>A
NM_002190.3:c.27+77T>A MANE Select NP_002181.1:n.27+77T>A
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