Canonical Allele Identifier: CA2679063643
Gene: IL17A HGNC NCBI

Linked Data

gnomAD v4: 6-52186407-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186407C>T , CM000668.2:g.52186407C>T GRCh38
NC_000006.11:g.52051205C>T , CM000668.1:g.52051205C>T GRCh37
NC_000006.10:g.52159164C>T NCBI36
NG_033021.1:g.5021C>T

Transcript Alleles

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