Canonical Allele Identifier: CA1089007538
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs1763288067
gnomAD v3: 6-52186518-C-G
gnomAD v4: 6-52186518-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186518C>G , CM000668.2:g.52186518C>G GRCh38
NC_000006.11:g.52051316C>G , CM000668.1:g.52051316C>G GRCh37
NC_000006.10:g.52159275C>G NCBI36
NG_033021.1:g.5132C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.27+60C>G MANE Select ENSP00000497968.1:n.27+60C>G
ENST00000340057.1:c.27+60C>G ENSP00000344192.1:n.27+60C>G
NM_002190.2:c.27+60C>G NP_002181.1:n.27+60C>G
NM_002190.3:c.27+60C>G MANE Select NP_002181.1:n.27+60C>G
Search 100 bp 5'
Search 100 bp 3'