Canonical Allele Identifier: CA229900
Gene: NLRC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 102937
ClinVar RCV Id: RCV000089197
dbSNP Id: rs199475951
gnomAD v2: 2-32490843-T-C
gnomAD v3: 2-32265774-T-C
gnomAD v4: 2-32265774-T-C
MyVariant Identifiers: chr2:g.32490843T>C (hg19) chr2:g.32265774T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32265774T>C , CM000664.2:g.32265774T>C GRCh38
NC_000002.11:g.32490843T>C , CM000664.1:g.32490843T>C GRCh37
NC_000002.10:g.32344347T>C NCBI36
NG_041780.1:g.4970A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000404025.2:c.-409A>G ENSP00000385090.2:n.-409A>G
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