Canonical Allele Identifier: CA364435342
Gene: IL17A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186456G>C , CM000668.2:g.52186456G>C GRCh38
NC_000006.11:g.52051254G>C , CM000668.1:g.52051254G>C GRCh37
NC_000006.10:g.52159213G>C NCBI36
NG_033021.1:g.5070G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.25G>C MANE Select ENSP00000497968.1:p.Val9Leu
ENST00000340057.1:c.25G>C ENSP00000344192.1:p.Val9Leu
NM_002190.2:c.25G>C NP_002181.1:p.Val9Leu
NM_002190.3:c.25G>C MANE Select NP_002181.1:p.Val9Leu