Canonical Allele Identifier: CA112100362
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs190909893
gnomAD v2: 4-187006446-A-C
gnomAD v3: 4-186085292-A-C
gnomAD v4: 4-186085292-A-C
MyVariant Identifiers: chr4:g.187006446A>C (hg19) chr4:g.186085292A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085292A>C , CM000666.2:g.186085292A>C GRCh38
NC_000004.11:g.187006446A>C , CM000666.1:g.187006446A>C GRCh37
NC_000004.10:g.187243440A>C NCBI36
NG_007278.1:g.21138A>C , LRG_117:g.21138A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*2686A>C ENSP00000513675.1:n.*2686A>C
ENST00000698353.1:n.3009A>C
ENST00000698354.1:c.*419A>C ENSP00000513676.1:n.*419A>C
ENST00000296795.8:c.*419A>C MANE Select ENSP00000296795.3:n.*419A>C
ENST00000296795.7:c.*419A>C ENSP00000296795.2:n.*419A>C
NM_003265.3:c.*419A>C MANE Select NP_003256.1:n.*419A>C
Search 100 bp 5'
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