Canonical Allele Identifier: CA792306716
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1371866950
gnomAD v3: 4-186085192-G-T
gnomAD v4: 4-186085192-G-T
MyVariant Identifiers: chr4:g.187006346G>T (hg19) chr4:g.186085192G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085192G>T , CM000666.2:g.186085192G>T GRCh38
NC_000004.11:g.187006346G>T , CM000666.1:g.187006346G>T GRCh37
NC_000004.10:g.187243340G>T NCBI36
NG_007278.1:g.21038G>T , LRG_117:g.21038G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*2586G>T ENSP00000513675.1:n.*2586G>T
ENST00000698353.1:n.2909G>T
ENST00000698354.1:c.*319G>T ENSP00000513676.1:n.*319G>T
ENST00000296795.8:c.*319G>T MANE Select ENSP00000296795.3:n.*319G>T
ENST00000296795.7:c.*319G>T ENSP00000296795.2:n.*319G>T
NM_003265.3:c.*319G>T MANE Select NP_003256.1:n.*319G>T
Search 100 bp 5'
Search 100 bp 3'