Canonical Allele Identifier: CA1628674713
Gene: IL17A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186438C= , CM000668.2:g.52186438C= GRCh38
NC_000006.11:g.52051236C= , CM000668.1:g.52051236C= GRCh37
NC_000006.10:g.52159195C= NCBI36
NG_033021.1:g.5052C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.7C= MANE Select ENSP00000497968.1:p.Pro3=
ENST00000340057.1:c.7C= ENSP00000344192.1:p.Pro3=
NM_002190.2:c.7C= NP_002181.1:p.Pro3=
NM_002190.3:c.7C= MANE Select NP_002181.1:p.Pro3=