Canonical Allele Identifier: CA138931565
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs3804513
gnomAD v2: 6-52053197-A-T
gnomAD v3: 6-52188399-A-T
gnomAD v4: 6-52188399-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52188399A>T , CM000668.2:g.52188399A>T GRCh38
NC_000006.11:g.52053197A>T , CM000668.1:g.52053197A>T GRCh37
NC_000006.10:g.52161156A>T NCBI36
NG_033021.1:g.7013A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.230+594A>T MANE Select ENSP00000497968.1:n.230+594A>T
ENST00000340057.1:c.230+594A>T ENSP00000344192.1:n.230+594A>T
NM_002190.2:c.230+594A>T NP_002181.1:n.230+594A>T
NM_002190.3:c.230+594A>T MANE Select NP_002181.1:n.230+594A>T