Canonical Allele Identifier: CA792327396
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1438112462
gnomAD v3: 4-186079244-TG-T
gnomAD v4: 4-186079244-TG-T
MyVariant Identifiers: chr4:g.187000399del (hg19) chr4:g.186079245del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186079247del , CM000666.2:g.186079247del GRCh38
NC_000004.11:g.187000401del , CM000666.1:g.187000401del GRCh37
NC_000004.10:g.187237395del NCBI36
NG_007278.1:g.15093del , LRG_117:g.15093del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698351.1:c.633+216del ENSP00000513674.1:n.633+216del
ENST00000698352.1:c.*185+216del ENSP00000513675.1:n.*185+216del
ENST00000296795.8:c.633+216del MANE Select ENSP00000296795.3:n.633+216del
ENST00000296795.7:c.633+216del ENSP00000296795.2:n.633+216del
ENST00000513189.1:c.633+216del ENSP00000423386.1:n.633+216del
NM_003265.2:c.633+216del , LRG_117t1:c.633+216del NP_003256.1:n.633+216del
NM_003265.3:c.633+216del MANE Select NP_003256.1:n.633+216del
Search 100 bp 5'
Search 100 bp 3'