Canonical Allele Identifier: CA1628674708
Gene: IL17A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186435A= , CM000668.2:g.52186435A= GRCh38
NC_000006.11:g.52051233A= , CM000668.1:g.52051233A= GRCh37
NC_000006.10:g.52159192A= NCBI36
NG_033021.1:g.5049A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.4A= MANE Select ENSP00000497968.1:p.Thr2=
ENST00000340057.1:c.4A= ENSP00000344192.1:p.Thr2=
NM_002190.2:c.4A= NP_002181.1:p.Thr2=
NM_002190.3:c.4A= MANE Select NP_002181.1:p.Thr2=
Search 100 bp 5'
Search 100 bp 3'