Canonical Allele Identifier: CA1628674803
Gene: IL17A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186457T= , CM000668.2:g.52186457T= GRCh38
NC_000006.11:g.52051255T= , CM000668.1:g.52051255T= GRCh37
NC_000006.10:g.52159214T= NCBI36
NG_033021.1:g.5071T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.26T= MANE Select ENSP00000497968.1:p.Val9=
ENST00000340057.1:c.26T= ENSP00000344192.1:p.Val9=
NM_002190.2:c.26T= NP_002181.1:p.Val9=
NM_002190.3:c.26T= MANE Select NP_002181.1:p.Val9=