Canonical Allele Identifier: CA2679063631
Gene: IL17A HGNC NCBI

Linked Data

gnomAD v4: 6-52186380-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186380T>C , CM000668.2:g.52186380T>C GRCh38
NC_000006.11:g.52051178T>C , CM000668.1:g.52051178T>C GRCh37
NC_000006.10:g.52159137T>C NCBI36
NG_033021.1:g.4994T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.-52T>C MANE Select ENSP00000497968.1:n.-52T>C
NM_002190.3:c.-52T>C MANE Select NP_002181.1:n.-52T>C
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