Canonical Allele Identifier: CA364435221

Gene: IL17A

Linked Data

• MyVariant Identifiers: chr6:g.52051249C>G (hg19) ; chr6:g.52186451C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52186451C>G , CM000668.2:g.52186451C>G	GRCh38
NC_000006.11:g.52051249C>G , CM000668.1:g.52051249C>G	GRCh37
NC_000006.10:g.52159208C>G	NCBI36
NG_033021.1:g.5065C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648244.1:c.20C>G MANE Select	ENSP00000497968.1:p.Ser7Ter
ENST00000340057.1:c.20C>G	ENSP00000344192.1:p.Ser7Ter
NM_002190.2:c.20C>G	NP_002181.1:p.Ser7Ter
NM_002190.3:c.20C>G MANE Select	NP_002181.1:p.Ser7Ter