Canonical Allele Identifier: CA450421988
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs1187468917
gnomAD v2: 6-52051253-G-A
MyVariant Identifiers: chr6:g.52051253G>A (hg19) chr6:g.52186455G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186455G>A , CM000668.2:g.52186455G>A GRCh38
NC_000006.11:g.52051253G>A , CM000668.1:g.52051253G>A GRCh37
NC_000006.10:g.52159212G>A NCBI36
NG_033021.1:g.5069G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.24G>A MANE Select ENSP00000497968.1:p.Leu8=
ENST00000340057.1:c.24G>A ENSP00000344192.1:p.Leu8=
NM_002190.2:c.24G>A NP_002181.1:p.Leu8=
NM_002190.3:c.24G>A MANE Select NP_002181.1:p.Leu8=
Search 100 bp 5'
Search 100 bp 3'