Canonical Allele Identifier: CA1628674882
Gene: IL17A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186501C= , CM000668.2:g.52186501C= GRCh38
NC_000006.11:g.52051299C= , CM000668.1:g.52051299C= GRCh37
NC_000006.10:g.52159258C= NCBI36
NG_033021.1:g.5115C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.27+43C= MANE Select ENSP00000497968.1:n.27+43C=
ENST00000340057.1:c.27+43C= ENSP00000344192.1:n.27+43C=
NM_002190.2:c.27+43C= NP_002181.1:n.27+43C=
NM_002190.3:c.27+43C= MANE Select NP_002181.1:n.27+43C=
Search 100 bp 5'
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