Canonical Allele Identifier: CA2679089708
Gene: IL17A HGNC NCBI

Linked Data

gnomAD v4: 6-52186539-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186539T>C , CM000668.2:g.52186539T>C GRCh38
NC_000006.11:g.52051337T>C , CM000668.1:g.52051337T>C GRCh37
NC_000006.10:g.52159296T>C NCBI36
NG_033021.1:g.5153T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.27+81T>C MANE Select ENSP00000497968.1:n.27+81T>C
ENST00000340057.1:c.27+81T>C ENSP00000344192.1:n.27+81T>C
NM_002190.2:c.27+81T>C NP_002181.1:n.27+81T>C
NM_002190.3:c.27+81T>C MANE Select NP_002181.1:n.27+81T>C
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