Canonical Allele Identifier: CA112100885
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs764811370

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085950C>T , CM000666.2:g.186085950C>T GRCh38
NC_000004.11:g.187007104C>T , CM000666.1:g.187007104C>T GRCh37
NC_000004.10:g.187244098C>T NCBI36
NG_007278.1:g.21796C>T , LRG_117:g.21796C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*3344C>T ENSP00000513675.1:n.*3344C>T
ENST00000698353.1:n.3667C>T
ENST00000698354.1:c.*1077C>T ENSP00000513676.1:n.*1077C>T
ENST00000296795.8:c.*1077C>T MANE Select ENSP00000296795.3:n.*1077C>T
ENST00000296795.7:c.*1077C>T ENSP00000296795.2:n.*1077C>T
NM_003265.3:c.*1077C>T MANE Select NP_003256.1:n.*1077C>T