Canonical Allele Identifier: CA112100466
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1014873185
gnomAD v4: 4-186085388-G-A
MyVariant Identifiers: chr4:g.187006542G>A (hg19) chr4:g.186085388G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085388G>A , CM000666.2:g.186085388G>A GRCh38
NC_000004.11:g.187006542G>A , CM000666.1:g.187006542G>A GRCh37
NC_000004.10:g.187243536G>A NCBI36
NG_007278.1:g.21234G>A , LRG_117:g.21234G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*2782G>A ENSP00000513675.1:n.*2782G>A
ENST00000698353.1:n.3105G>A
ENST00000698354.1:c.*515G>A ENSP00000513676.1:n.*515G>A
ENST00000296795.8:c.*515G>A MANE Select ENSP00000296795.3:n.*515G>A
ENST00000296795.7:c.*515G>A ENSP00000296795.2:n.*515G>A
NM_003265.3:c.*515G>A MANE Select NP_003256.1:n.*515G>A
Search 100 bp 5'
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