Canonical Allele Identifier: CA112100625
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs765024605
MyVariant Identifiers: chr4:g.187006902A>G (hg19) chr4:g.186085748A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085748A>G , CM000666.2:g.186085748A>G GRCh38
NC_000004.11:g.187006902A>G , CM000666.1:g.187006902A>G GRCh37
NC_000004.10:g.187243896A>G NCBI36
NG_007278.1:g.21594A>G , LRG_117:g.21594A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000698352.1:c.*3142A>G ENSP00000513675.1:n.*3142A>G
ENST00000698353.1:n.3465A>G
ENST00000698354.1:c.*875A>G ENSP00000513676.1:n.*875A>G
ENST00000296795.8:c.*875A>G MANE Select ENSP00000296795.3:n.*875A>G
ENST00000296795.7:c.*875A>G ENSP00000296795.2:n.*875A>G
NM_003265.3:c.*875A>G MANE Select NP_003256.1:n.*875A>G
Search 100 bp 5'
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