Canonical Allele Identifier: CA112538879
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1006436691
gnomAD v3: 4-186069886-C-A
gnomAD v4: 4-186069886-C-A
MyVariant Identifiers: chr4:g.186991040C>A (hg19) chr4:g.186069886C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186069886C>A , CM000666.2:g.186069886C>A GRCh38
NC_000004.11:g.186991040C>A , CM000666.1:g.186991040C>A GRCh37
NC_000004.10:g.187228034C>A NCBI36
NG_007278.1:g.5732C>A , LRG_117:g.5732C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698351.1:c.-8+638C>A ENSP00000513674.1:n.-8+638C>A
ENST00000698352.1:c.-8+638C>A ENSP00000513675.1:n.-8+638C>A
ENST00000296795.8:c.-8+638C>A MANE Select ENSP00000296795.3:n.-8+638C>A
ENST00000296795.7:c.-8+638C>A ENSP00000296795.2:n.-8+638C>A
ENST00000513189.1:c.-8+638C>A ENSP00000423386.1:n.-8+638C>A
NM_003265.2:c.-8+638C>A , LRG_117t1:c.-8+638C>A NP_003256.1:n.-8+638C>A
NM_003265.3:c.-8+638C>A MANE Select NP_003256.1:n.-8+638C>A
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