Canonical Allele Identifier: CA112100508
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs187868236
gnomAD v2: 4-187006694-C-G
gnomAD v3: 4-186085540-C-G
gnomAD v4: 4-186085540-C-G
MyVariant Identifiers: chr4:g.187006694C>G (hg19) chr4:g.186085540C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085540C>G , CM000666.2:g.186085540C>G GRCh38
NC_000004.11:g.187006694C>G , CM000666.1:g.187006694C>G GRCh37
NC_000004.10:g.187243688C>G NCBI36
NG_007278.1:g.21386C>G , LRG_117:g.21386C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*2934C>G ENSP00000513675.1:n.*2934C>G
ENST00000698353.1:n.3257C>G
ENST00000698354.1:c.*667C>G ENSP00000513676.1:n.*667C>G
ENST00000296795.8:c.*667C>G MANE Select ENSP00000296795.3:n.*667C>G
ENST00000296795.7:c.*667C>G ENSP00000296795.2:n.*667C>G
NM_003265.3:c.*667C>G MANE Select NP_003256.1:n.*667C>G
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