Canonical Allele Identifier: CA1628674980
Gene: IL17A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186536G= , CM000668.2:g.52186536G= GRCh38
NC_000006.11:g.52051334G= , CM000668.1:g.52051334G= GRCh37
NC_000006.10:g.52159293G= NCBI36
NG_033021.1:g.5150G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.27+78G= MANE Select ENSP00000497968.1:n.27+78G=
ENST00000340057.1:c.27+78G= ENSP00000344192.1:n.27+78G=
NM_002190.2:c.27+78G= NP_002181.1:n.27+78G=
NM_002190.3:c.27+78G= MANE Select NP_002181.1:n.27+78G=