Canonical Allele Identifier: CA1071967727
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs113814587
gnomAD v3: 4-186085903-C-G
gnomAD v4: 4-186085903-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085903C>G , CM000666.2:g.186085903C>G GRCh38
NC_000004.11:g.187007057C>G , CM000666.1:g.187007057C>G GRCh37
NC_000004.10:g.187244051C>G NCBI36
NG_007278.1:g.21749C>G , LRG_117:g.21749C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*3297C>G ENSP00000513675.1:n.*3297C>G
ENST00000698353.1:n.3620C>G
ENST00000698354.1:c.*1030C>G ENSP00000513676.1:n.*1030C>G
ENST00000296795.8:c.*1030C>G MANE Select ENSP00000296795.3:n.*1030C>G
ENST00000296795.7:c.*1030C>G ENSP00000296795.2:n.*1030C>G
NM_003265.3:c.*1030C>G MANE Select NP_003256.1:n.*1030C>G
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