Canonical Allele Identifier: CA792306938
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1489656338
MyVariant Identifiers: chr4:g.187006658A>G (hg19) chr4:g.186085504A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085504A>G , CM000666.2:g.186085504A>G GRCh38
NC_000004.11:g.187006658A>G , CM000666.1:g.187006658A>G GRCh37
NC_000004.10:g.187243652A>G NCBI36
NG_007278.1:g.21350A>G , LRG_117:g.21350A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000698352.1:c.*2898A>G ENSP00000513675.1:n.*2898A>G
ENST00000698353.1:n.3221A>G
ENST00000698354.1:c.*631A>G ENSP00000513676.1:n.*631A>G
ENST00000296795.8:c.*631A>G MANE Select ENSP00000296795.3:n.*631A>G
ENST00000296795.7:c.*631A>G ENSP00000296795.2:n.*631A>G
NM_003265.3:c.*631A>G MANE Select NP_003256.1:n.*631A>G
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