Canonical Allele Identifier: CA364435165
Gene: IL17A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186447A>G , CM000668.2:g.52186447A>G GRCh38
NC_000006.11:g.52051245A>G , CM000668.1:g.52051245A>G GRCh37
NC_000006.10:g.52159204A>G NCBI36
NG_033021.1:g.5061A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.16A>G MANE Select ENSP00000497968.1:p.Thr6Ala
ENST00000340057.1:c.16A>G ENSP00000344192.1:p.Thr6Ala
NM_002190.2:c.16A>G NP_002181.1:p.Thr6Ala
NM_002190.3:c.16A>G MANE Select NP_002181.1:p.Thr6Ala