Canonical Allele Identifier: CA364435324
Gene: IL17A HGNC NCBI

Linked Data

gnomAD v4: 6-52186455-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186455G>T , CM000668.2:g.52186455G>T GRCh38
NC_000006.11:g.52051253G>T , CM000668.1:g.52051253G>T GRCh37
NC_000006.10:g.52159212G>T NCBI36
NG_033021.1:g.5069G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.24G>T MANE Select ENSP00000497968.1:p.Leu8Phe
ENST00000340057.1:c.24G>T ENSP00000344192.1:p.Leu8Phe
NM_002190.2:c.24G>T NP_002181.1:p.Leu8Phe
NM_002190.3:c.24G>T MANE Select NP_002181.1:p.Leu8Phe