Canonical Allele Identifier: CA3854192
Gene: IL17A HGNC NCBI

Linked Data

ClinVar Variation Id: 1273159
ClinVar RCV Id: RCV001678982 RCV003487678
dbSNP Id: rs3819025
ExAC: 6:52051274 G / A
gnomAD v2: 6-52051274-G-A
gnomAD v3: 6-52186476-G-A
gnomAD v4: 6-52186476-G-A
MyVariant Identifiers: chr6:g.52051274G>A (hg19) chr6:g.52186476G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186476G>A , CM000668.2:g.52186476G>A GRCh38
NC_000006.11:g.52051274G>A , CM000668.1:g.52051274G>A GRCh37
NC_000006.10:g.52159233G>A NCBI36
NG_033021.1:g.5090G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.27+18G>A MANE Select ENSP00000497968.1:n.27+18G>A
ENST00000340057.1:c.27+18G>A ENSP00000344192.1:n.27+18G>A
NM_002190.2:c.27+18G>A NP_002181.1:n.27+18G>A
NM_002190.3:c.27+18G>A MANE Select NP_002181.1:n.27+18G>A
Search 100 bp 5'
Search 100 bp 3'