Canonical Allele Identifier: CA450421976
Gene: IL17A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.52051235T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186437T>G , CM000668.2:g.52186437T>G GRCh38
NC_000006.11:g.52051235T>G , CM000668.1:g.52051235T>G GRCh37
NC_000006.10:g.52159194T>G NCBI36
NG_033021.1:g.5051T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.6T>G MANE Select ENSP00000497968.1:p.Thr2=
ENST00000340057.1:c.6T>G ENSP00000344192.1:p.Thr2=
NM_002190.2:c.6T>G NP_002181.1:p.Thr2=
NM_002190.3:c.6T>G MANE Select NP_002181.1:p.Thr2=
Search 100 bp 5'
Search 100 bp 3'