Canonical Allele Identifier: CA557044459
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1402200875
gnomAD v2: 4-187006950-AT-A
gnomAD v3: 4-186085796-AT-A
gnomAD v4: 4-186085796-AT-A
MyVariant Identifiers: chr4:g.187006951del (hg19) chr4:g.186085797del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085797del , CM000666.2:g.186085797del GRCh38
NC_000004.11:g.187006951del , CM000666.1:g.187006951del GRCh37
NC_000004.10:g.187243945del NCBI36
NG_007278.1:g.21643del , LRG_117:g.21643del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*3191del ENSP00000513675.1:n.*3191del
ENST00000698353.1:n.3514del
ENST00000698354.1:c.*924del ENSP00000513676.1:n.*924del
ENST00000296795.8:c.*924del MANE Select ENSP00000296795.3:n.*924del
ENST00000296795.7:c.*924del ENSP00000296795.2:n.*924del
NM_003265.3:c.*924del MANE Select NP_003256.1:n.*924del
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