Canonical Allele Identifier: CA364435184
Gene: IL17A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186448C>A , CM000668.2:g.52186448C>A GRCh38
NC_000006.11:g.52051246C>A , CM000668.1:g.52051246C>A GRCh37
NC_000006.10:g.52159205C>A NCBI36
NG_033021.1:g.5062C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.17C>A MANE Select ENSP00000497968.1:p.Thr6Asn
ENST00000340057.1:c.17C>A ENSP00000344192.1:p.Thr6Asn
NM_002190.2:c.17C>A NP_002181.1:p.Thr6Asn
NM_002190.3:c.17C>A MANE Select NP_002181.1:p.Thr6Asn