Canonical Allele Identifier: CA112101044
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1020993313
gnomAD v3: 4-186086088-T-G
gnomAD v4: 4-186086088-T-G
MyVariant Identifiers: chr4:g.187007242T>G (hg19) chr4:g.186086088T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186086088T>G , CM000666.2:g.186086088T>G GRCh38
NC_000004.11:g.187007242T>G , CM000666.1:g.187007242T>G GRCh37
NC_000004.10:g.187244236T>G NCBI36
NG_007278.1:g.21934T>G , LRG_117:g.21934T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*3482T>G ENSP00000513675.1:n.*3482T>G
ENST00000698353.1:n.3805T>G
ENST00000698354.1:c.*1215T>G ENSP00000513676.1:n.*1215T>G
ENST00000296795.8:c.*1215T>G MANE Select ENSP00000296795.3:n.*1215T>G
ENST00000296795.7:c.*1215T>G ENSP00000296795.2:n.*1215T>G
NM_003265.3:c.*1215T>G MANE Select NP_003256.1:n.*1215T>G
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