Canonical Allele Identifier: CA792306853
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1444982420
gnomAD v3: 4-186085384-CT-C
gnomAD v4: 4-186085384-CT-C
MyVariant Identifiers: chr4:g.187006539del (hg19) chr4:g.186085385del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085387del , CM000666.2:g.186085387del GRCh38
NC_000004.11:g.187006541del , CM000666.1:g.187006541del GRCh37
NC_000004.10:g.187243535del NCBI36
NG_007278.1:g.21233del , LRG_117:g.21233del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*2781del ENSP00000513675.1:n.*2781del
ENST00000698353.1:n.3104del
ENST00000698354.1:c.*514del ENSP00000513676.1:n.*514del
ENST00000296795.8:c.*514del MANE Select ENSP00000296795.3:n.*514del
ENST00000296795.7:c.*514del ENSP00000296795.2:n.*514del
NM_003265.3:c.*514del MANE Select NP_003256.1:n.*514del
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