Canonical Allele Identifier: CA1628674838
Gene: IL17A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186469C= , CM000668.2:g.52186469C= GRCh38
NC_000006.11:g.52051267C= , CM000668.1:g.52051267C= GRCh37
NC_000006.10:g.52159226C= NCBI36
NG_033021.1:g.5083C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.27+11C= MANE Select ENSP00000497968.1:n.27+11C=
ENST00000340057.1:c.27+11C= ENSP00000344192.1:n.27+11C=
NM_002190.2:c.27+11C= NP_002181.1:n.27+11C=
NM_002190.3:c.27+11C= MANE Select NP_002181.1:n.27+11C=