Canonical Allele Identifier: CA1628674578
Gene: IL17A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186385T= , CM000668.2:g.52186385T= GRCh38
NC_000006.11:g.52051183T= , CM000668.1:g.52051183T= GRCh37
NC_000006.10:g.52159142T= NCBI36
NG_033021.1:g.4999T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.-47T= MANE Select ENSP00000497968.1:n.-47T=
NM_002190.3:c.-47T= MANE Select NP_002181.1:n.-47T=