Canonical Allele Identifier: CA112100739
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs149785773
gnomAD v2: 4-187006999-TG-T
gnomAD v3: 4-186085845-TG-T
gnomAD v4: 4-186085845-TG-T
MyVariant Identifiers: chr4:g.187007000del (hg19) chr4:g.186085846del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085846del , CM000666.2:g.186085846del GRCh38
NC_000004.11:g.187007000del , CM000666.1:g.187007000del GRCh37
NC_000004.10:g.187243994del NCBI36
NG_007278.1:g.21692del , LRG_117:g.21692del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*3240del ENSP00000513675.1:n.*3240del
ENST00000698353.1:n.3563del
ENST00000698354.1:c.*973del ENSP00000513676.1:n.*973del
ENST00000296795.8:c.*973del MANE Select ENSP00000296795.3:n.*973del
ENST00000296795.7:c.*973del ENSP00000296795.2:n.*973del
NM_003265.3:c.*973del MANE Select NP_003256.1:n.*973del
Search 100 bp 5'
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