Canonical Allele Identifier: CA112100438
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs528235177
MyVariant Identifiers: chr4:g.186085368C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085368C>G , CM000666.2:g.186085368C>G GRCh38
NC_000004.11:g.187006522C>G , CM000666.1:g.187006522C>G GRCh37
NC_000004.10:g.187243516C>G NCBI36
NG_007278.1:g.21214C>G , LRG_117:g.21214C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*2762C>G ENSP00000513675.1:n.*2762C>G
ENST00000698353.1:n.3085C>G
ENST00000698354.1:c.*495C>G ENSP00000513676.1:n.*495C>G
ENST00000296795.8:c.*495C>G MANE Select ENSP00000296795.3:n.*495C>G
ENST00000296795.7:c.*495C>G ENSP00000296795.2:n.*495C>G
NM_003265.3:c.*495C>G MANE Select NP_003256.1:n.*495C>G
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