Canonical Allele Identifier: CA792307235
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1197353186
gnomAD v3: 4-186086046-T-C
gnomAD v4: 4-186086046-T-C
MyVariant Identifiers: chr4:g.187007200T>C (hg19) chr4:g.186086046T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186086046T>C , CM000666.2:g.186086046T>C GRCh38
NC_000004.11:g.187007200T>C , CM000666.1:g.187007200T>C GRCh37
NC_000004.10:g.187244194T>C NCBI36
NG_007278.1:g.21892T>C , LRG_117:g.21892T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*3440T>C ENSP00000513675.1:n.*3440T>C
ENST00000698353.1:n.3763T>C
ENST00000698354.1:c.*1173T>C ENSP00000513676.1:n.*1173T>C
ENST00000296795.8:c.*1173T>C MANE Select ENSP00000296795.3:n.*1173T>C
ENST00000296795.7:c.*1173T>C ENSP00000296795.2:n.*1173T>C
NM_003265.3:c.*1173T>C MANE Select NP_003256.1:n.*1173T>C
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