Canonical Allele Identifier: CA364435271
Gene: IL17A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.52051252T>A (hg19) chr6:g.52186454T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186454T>A , CM000668.2:g.52186454T>A GRCh38
NC_000006.11:g.52051252T>A , CM000668.1:g.52051252T>A GRCh37
NC_000006.10:g.52159211T>A NCBI36
NG_033021.1:g.5068T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.23T>A MANE Select ENSP00000497968.1:p.Leu8Ter
ENST00000340057.1:c.23T>A ENSP00000344192.1:p.Leu8Ter
NM_002190.2:c.23T>A NP_002181.1:p.Leu8Ter
NM_002190.3:c.23T>A MANE Select NP_002181.1:p.Leu8Ter
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Search 100 bp 3'