Canonical Allele Identifier: CA112100866
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1052902850
MyVariant Identifiers: chr4:g.187007087C>T (hg19) chr4:g.186085933C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085933C>T , CM000666.2:g.186085933C>T GRCh38
NC_000004.11:g.187007087C>T , CM000666.1:g.187007087C>T GRCh37
NC_000004.10:g.187244081C>T NCBI36
NG_007278.1:g.21779C>T , LRG_117:g.21779C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*3327C>T ENSP00000513675.1:n.*3327C>T
ENST00000698353.1:n.3650C>T
ENST00000698354.1:c.*1060C>T ENSP00000513676.1:n.*1060C>T
ENST00000296795.8:c.*1060C>T MANE Select ENSP00000296795.3:n.*1060C>T
ENST00000296795.7:c.*1060C>T ENSP00000296795.2:n.*1060C>T
NM_003265.3:c.*1060C>T MANE Select NP_003256.1:n.*1060C>T
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