Canonical Allele Identifier: CA1628674680
Gene: IL17A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186418T= , CM000668.2:g.52186418T= GRCh38
NC_000006.11:g.52051216T= , CM000668.1:g.52051216T= GRCh37
NC_000006.10:g.52159175T= NCBI36
NG_033021.1:g.5032T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.-14T= MANE Select ENSP00000497968.1:n.-14T=
ENST00000340057.1:c.-14T= ENSP00000344192.1:n.-14T=
NM_002190.2:c.-14T= NP_002181.1:n.-14T=
NM_002190.3:c.-14T= MANE Select NP_002181.1:n.-14T=