Canonical Allele Identifier: CA364435059

Gene: IL17A

Linked Data

• MyVariant Identifiers: chr6:g.52051237C>A (hg19) ; chr6:g.52186439C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52186439C>A , CM000668.2:g.52186439C>A	GRCh38
NC_000006.11:g.52051237C>A , CM000668.1:g.52051237C>A	GRCh37
NC_000006.10:g.52159196C>A	NCBI36
NG_033021.1:g.5053C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648244.1:c.8C>A MANE Select	ENSP00000497968.1:p.Pro3His
ENST00000340057.1:c.8C>A	ENSP00000344192.1:p.Pro3His
NM_002190.2:c.8C>A	NP_002181.1:p.Pro3His
NM_002190.3:c.8C>A MANE Select	NP_002181.1:p.Pro3His