Canonical Allele Identifier: CA3854189
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs765164206
ExAC: 6:52051250 A / T
gnomAD v2: 6-52051250-A-T
gnomAD v3: 6-52186452-A-T
gnomAD v4: 6-52186452-A-T
MyVariant Identifiers: chr6:g.52051250A>T (hg19) chr6:g.52186452A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186452A>T , CM000668.2:g.52186452A>T GRCh38
NC_000006.11:g.52051250A>T , CM000668.1:g.52051250A>T GRCh37
NC_000006.10:g.52159209A>T NCBI36
NG_033021.1:g.5066A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.21A>T MANE Select ENSP00000497968.1:p.Ser7=
ENST00000340057.1:c.21A>T ENSP00000344192.1:p.Ser7=
NM_002190.2:c.21A>T NP_002181.1:p.Ser7=
NM_002190.3:c.21A>T MANE Select NP_002181.1:p.Ser7=
Search 100 bp 5'
Search 100 bp 3'