Canonical Allele Identifier: CA792327430
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1196697179
MyVariant Identifiers: chr4:g.187000431A>G (hg19) chr4:g.186079277A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186079277A>G , CM000666.2:g.186079277A>G GRCh38
NC_000004.11:g.187000431A>G , CM000666.1:g.187000431A>G GRCh37
NC_000004.10:g.187237425A>G NCBI36
NG_007278.1:g.15123A>G , LRG_117:g.15123A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000698351.1:c.633+246A>G ENSP00000513674.1:n.633+246A>G
ENST00000698352.1:c.*185+246A>G ENSP00000513675.1:n.*185+246A>G
ENST00000296795.8:c.633+246A>G MANE Select ENSP00000296795.3:n.633+246A>G
ENST00000296795.7:c.633+246A>G ENSP00000296795.2:n.633+246A>G
ENST00000513189.1:c.633+246A>G ENSP00000423386.1:n.633+246A>G
NM_003265.2:c.633+246A>G , LRG_117t1:c.633+246A>G NP_003256.1:n.633+246A>G
NM_003265.3:c.633+246A>G MANE Select NP_003256.1:n.633+246A>G
Search 100 bp 5'
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