Canonical Allele Identifier: CA3854180
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs751747356

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186410del , CM000668.2:g.52186410del GRCh38
NC_000006.11:g.52051208del , CM000668.1:g.52051208del GRCh37
NC_000006.10:g.52159167del NCBI36
NG_033021.1:g.5024del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.-22del MANE Select ENSP00000497968.1:n.-22del
ENST00000340057.1:c.-22del ENSP00000344192.1:n.-22del
NM_002190.2:c.-22del NP_002181.1:n.-22del
NM_002190.3:c.-22del MANE Select NP_002181.1:n.-22del