Canonical Allele Identifier: CA112101057
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs968212052
gnomAD v3: 4-186086103-A-T
gnomAD v4: 4-186086103-A-T
MyVariant Identifiers: chr4:g.187007257A>T (hg19) chr4:g.186086103A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186086103A>T , CM000666.2:g.186086103A>T GRCh38
NC_000004.11:g.187007257A>T , CM000666.1:g.187007257A>T GRCh37
NC_000004.10:g.187244251A>T NCBI36
NG_007278.1:g.21949A>T , LRG_117:g.21949A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*3497A>T ENSP00000513675.1:n.*3497A>T
ENST00000698353.1:n.3820A>T
ENST00000698354.1:c.*1230A>T ENSP00000513676.1:n.*1230A>T
ENST00000296795.8:c.*1230A>T MANE Select ENSP00000296795.3:n.*1230A>T
ENST00000296795.7:c.*1230A>T ENSP00000296795.2:n.*1230A>T
NM_003265.3:c.*1230A>T MANE Select NP_003256.1:n.*1230A>T
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