Canonical Allele Identifier: CA450421990
Gene: IL17A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.52051256G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186458G>C , CM000668.2:g.52186458G>C GRCh38
NC_000006.11:g.52051256G>C , CM000668.1:g.52051256G>C GRCh37
NC_000006.10:g.52159215G>C NCBI36
NG_033021.1:g.5072G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.27G>C MANE Select ENSP00000497968.1:p.Val9=
ENST00000340057.1:c.27G>C ENSP00000344192.1:p.Val9=
NM_002190.2:c.27G>C NP_002181.1:p.Val9=
NM_002190.3:c.27G>C MANE Select NP_002181.1:p.Val9=
Search 100 bp 5'
Search 100 bp 3'