Canonical Allele Identifier: CA1628674663
Gene: IL17A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186412G= , CM000668.2:g.52186412G= GRCh38
NC_000006.11:g.52051210G= , CM000668.1:g.52051210G= GRCh37
NC_000006.10:g.52159169G= NCBI36
NG_033021.1:g.5026G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.-20G= MANE Select ENSP00000497968.1:n.-20G=
ENST00000340057.1:c.-20G= ENSP00000344192.1:n.-20G=
NM_002190.2:c.-20G= NP_002181.1:n.-20G=
NM_002190.3:c.-20G= MANE Select NP_002181.1:n.-20G=