Canonical Allele Identifier: CA364434966

Gene: IL17A

Linked Data

• gnomAD v4: 6-52186432-A-G
• MyVariant Identifiers: chr6:g.52051230A>G (hg19) ; chr6:g.52186432A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52186432A>G , CM000668.2:g.52186432A>G	GRCh38
NC_000006.11:g.52051230A>G , CM000668.1:g.52051230A>G	GRCh37
NC_000006.10:g.52159189A>G	NCBI36
NG_033021.1:g.5046A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648244.1:c.1A>G MANE Select	ENSP00000497968.1:p.Met1Val
ENST00000340057.1:c.1A>G	ENSP00000344192.1:p.Met1Val
NM_002190.2:c.1A>G	NP_002181.1:p.Met1Val
NM_002190.3:c.1A>G MANE Select	NP_002181.1:p.Met1Val