Canonical Allele Identifier: CA3161135
Gene: TLR3 HGNC NCBI
COSMIC:
COSN8870240 (not active)
MyVariant.info:
GRCh38 chr4:g.186076613C>A
GRCh37 chr4:g.186997767C>A
gnomAD v2:
4:186997767 C / A
gnomAD v3:
4:186076613 C / A
gnomAD v4:
chr4-186076613-C-A
Joint Max Group AF 0.25405991 (EAS)
Genomes Max Group AF 0.23752521 (EAS)
Exomes Max Group AF 0.25499327 (EAS)
ClinVar RCV:
RCV001515649
RCV003487346
ClinVar Variation:
1166908
dbSNP:
3775296
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186076613C>A , CM000666.2:g.186076613C>A GRCh38
NC_000004.11:g.186997767C>A , CM000666.1:g.186997767C>A GRCh37
NC_000004.10:g.187234761C>A NCBI36
NG_007278.1:g.12459C>A , LRG_117:g.12459C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698351.1:c.-7C>A ENSP00000513674.1:n.-7C>A
ENST00000698352.1:c.-7C>A ENSP00000513675.1:n.-7C>A
ENST00000296795.8:c.-7C>A MANE Select ENSP00000296795.3:n.-7C>A
ENST00000296795.7:c.-7C>A ENSP00000296795.2:n.-7C>A
ENST00000513189.1:c.-7C>A ENSP00000423386.1:n.-7C>A
NM_003265.2:c.-7C>A , LRG_117t1:c.-7C>A NP_003256.1:n.-7C>A
NM_003265.3:c.-7C>A MANE Select NP_003256.1:n.-7C>A
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