Canonical Allele Identifier: CA1089007535
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs140425841
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186500C>A , CM000668.2:g.52186500C>A GRCh38
NC_000006.11:g.52051298C>A , CM000668.1:g.52051298C>A GRCh37
NC_000006.10:g.52159257C>A NCBI36
NG_033021.1:g.5114C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.27+42C>A MANE Select ENSP00000497968.1:n.27+42C>A
ENST00000340057.1:c.27+42C>A ENSP00000344192.1:n.27+42C>A
NM_002190.2:c.27+42C>A NP_002181.1:n.27+42C>A
NM_002190.3:c.27+42C>A MANE Select NP_002181.1:n.27+42C>A
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