Canonical Allele Identifier: CA138929531
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs199815459
gnomAD v3: 6-52186440-T-G
gnomAD v4: 6-52186440-T-G
MyVariant Identifiers: chr6:g.52051238T>G (hg19) chr6:g.52186440T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186440T>G , CM000668.2:g.52186440T>G GRCh38
NC_000006.11:g.52051238T>G , CM000668.1:g.52051238T>G GRCh37
NC_000006.10:g.52159197T>G NCBI36
NG_033021.1:g.5054T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.9T>G MANE Select ENSP00000497968.1:p.Pro3=
ENST00000340057.1:c.9T>G ENSP00000344192.1:p.Pro3=
NM_002190.2:c.9T>G NP_002181.1:p.Pro3=
NM_002190.3:c.9T>G MANE Select NP_002181.1:p.Pro3=
Search 100 bp 5'
Search 100 bp 3'