Canonical Allele Identifier: CA112539829
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs946903404
gnomAD v3: 4-186079133-T-C
gnomAD v4: 4-186079133-T-C
MyVariant Identifiers: chr4:g.186079133T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186079133T>C , CM000666.2:g.186079133T>C GRCh38
NC_000004.11:g.187000287T>C , CM000666.1:g.187000287T>C GRCh37
NC_000004.10:g.187237281T>C NCBI36
NG_007278.1:g.14979T>C , LRG_117:g.14979T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698351.1:c.633+102T>C ENSP00000513674.1:n.633+102T>C
ENST00000698352.1:c.*185+102T>C ENSP00000513675.1:n.*185+102T>C
ENST00000296795.8:c.633+102T>C MANE Select ENSP00000296795.3:n.633+102T>C
ENST00000296795.7:c.633+102T>C ENSP00000296795.2:n.633+102T>C
ENST00000513189.1:c.633+102T>C ENSP00000423386.1:n.633+102T>C
NM_003265.2:c.633+102T>C , LRG_117t1:c.633+102T>C NP_003256.1:n.633+102T>C
NM_003265.3:c.633+102T>C MANE Select NP_003256.1:n.633+102T>C
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