Canonical Allele Identifier: CA112100368
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs955285310
MyVariant Identifiers: chr4:g.187006468A>G (hg19) chr4:g.186085314A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085314A>G , CM000666.2:g.186085314A>G GRCh38
NC_000004.11:g.187006468A>G , CM000666.1:g.187006468A>G GRCh37
NC_000004.10:g.187243462A>G NCBI36
NG_007278.1:g.21160A>G , LRG_117:g.21160A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*2708A>G ENSP00000513675.1:n.*2708A>G
ENST00000698353.1:n.3031A>G
ENST00000698354.1:c.*441A>G ENSP00000513676.1:n.*441A>G
ENST00000296795.8:c.*441A>G MANE Select ENSP00000296795.3:n.*441A>G
ENST00000296795.7:c.*441A>G ENSP00000296795.2:n.*441A>G
NM_003265.3:c.*441A>G MANE Select NP_003256.1:n.*441A>G
Search 100 bp 5'
Search 100 bp 3'