Canonical Allele Identifier: CA112100638
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs895536762
gnomAD v3: 4-186085751-G-A
gnomAD v4: 4-186085751-G-A
MyVariant Identifiers: chr4:g.187006905G>A (hg19) chr4:g.186085751G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085751G>A , CM000666.2:g.186085751G>A GRCh38
NC_000004.11:g.187006905G>A , CM000666.1:g.187006905G>A GRCh37
NC_000004.10:g.187243899G>A NCBI36
NG_007278.1:g.21597G>A , LRG_117:g.21597G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*3145G>A ENSP00000513675.1:n.*3145G>A
ENST00000698353.1:n.3468G>A
ENST00000698354.1:c.*878G>A ENSP00000513676.1:n.*878G>A
ENST00000296795.8:c.*878G>A MANE Select ENSP00000296795.3:n.*878G>A
ENST00000296795.7:c.*878G>A ENSP00000296795.2:n.*878G>A
NM_003265.3:c.*878G>A MANE Select NP_003256.1:n.*878G>A
Search 100 bp 5'
Search 100 bp 3'