Canonical Allele Identifier: CA825771996
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs1223736427
gnomAD v3: 6-52186422-A-G
gnomAD v4: 6-52186422-A-G
MyVariant Identifiers: chr6:g.52051220A>G (hg19) chr6:g.52186422A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186422A>G , CM000668.2:g.52186422A>G GRCh38
NC_000006.11:g.52051220A>G , CM000668.1:g.52051220A>G GRCh37
NC_000006.10:g.52159179A>G NCBI36
NG_033021.1:g.5036A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.-10A>G MANE Select ENSP00000497968.1:n.-10A>G
ENST00000340057.1:c.-10A>G ENSP00000344192.1:n.-10A>G
NM_002190.2:c.-10A>G NP_002181.1:n.-10A>G
NM_002190.3:c.-10A>G MANE Select NP_002181.1:n.-10A>G
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