Canonical Allele Identifier: CA3854178
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs375071669
gnomAD v2: 6-52051200-T-C
gnomAD v3: 6-52186402-T-C
gnomAD v4: 6-52186402-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186402T>C , CM000668.2:g.52186402T>C GRCh38
NC_000006.11:g.52051200T>C , CM000668.1:g.52051200T>C GRCh37
NC_000006.10:g.52159159T>C NCBI36
NG_033021.1:g.5016T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.-30T>C MANE Select ENSP00000497968.1:n.-30T>C
ENST00000340057.1:c.-30T>C ENSP00000344192.1:n.-30T>C
NM_002190.2:c.-30T>C NP_002181.1:n.-30T>C
NM_002190.3:c.-30T>C MANE Select NP_002181.1:n.-30T>C