Canonical Allele Identifier: CA16445246
Gene: IL23A HGNC NCBI

Linked Data

dbSNP Id: rs2371494
gnomAD v2: 12-56728000-G-A
gnomAD v3: 12-56334216-G-A
gnomAD v4: 12-56334216-G-A
MyVariant Identifiers: chr12:g.56728000G>A (hg19) chr12:g.56334216G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56334216G>A , CM000674.2:g.56334216G>A GRCh38
NC_000012.11:g.56728000G>A , CM000674.1:g.56728000G>A GRCh37
NC_000012.10:g.55014267G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000619177.1:n.9G>A
ENST00000622119.4:n.43G>A
XM_011538477.1:c.-296G>A XP_011536779.1:n.-296G>A
XM_011538477.2:c.-296G>A XP_011536779.1:n.-296G>A
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