Canonical Allele Identifier: CA112539856
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs780017425
gnomAD v2: 4-187000468-A-C
gnomAD v3: 4-186079314-A-C
gnomAD v4: 4-186079314-A-C
MyVariant Identifiers: chr4:g.187000468A>C (hg19) chr4:g.186079314A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186079314A>C , CM000666.2:g.186079314A>C GRCh38
NC_000004.11:g.187000468A>C , CM000666.1:g.187000468A>C GRCh37
NC_000004.10:g.187237462A>C NCBI36
NG_007278.1:g.15160A>C , LRG_117:g.15160A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698351.1:c.633+283A>C ENSP00000513674.1:n.633+283A>C
ENST00000698352.1:c.*185+283A>C ENSP00000513675.1:n.*185+283A>C
ENST00000296795.8:c.633+283A>C MANE Select ENSP00000296795.3:n.633+283A>C
ENST00000296795.7:c.633+283A>C ENSP00000296795.2:n.633+283A>C
ENST00000513189.1:c.633+283A>C ENSP00000423386.1:n.633+283A>C
NM_003265.2:c.633+283A>C , LRG_117t1:c.633+283A>C NP_003256.1:n.633+283A>C
NM_003265.3:c.633+283A>C MANE Select NP_003256.1:n.633+283A>C
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