Canonical Allele Identifier: CA1628674577
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs1763284291
gnomAD v4: 6-52186385-T-A

Genomic Alleles

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

Transcript Alleles

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