Canonical Allele Identifier: CA112538882
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs973079001

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186069925T>C , CM000666.2:g.186069925T>C GRCh38
NC_000004.11:g.186991079T>C , CM000666.1:g.186991079T>C GRCh37
NC_000004.10:g.187228073T>C NCBI36
NG_007278.1:g.5771T>C , LRG_117:g.5771T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698351.1:c.-8+677T>C ENSP00000513674.1:n.-8+677T>C
ENST00000698352.1:c.-8+677T>C ENSP00000513675.1:n.-8+677T>C
ENST00000296795.8:c.-8+677T>C MANE Select ENSP00000296795.3:n.-8+677T>C
ENST00000296795.7:c.-8+677T>C ENSP00000296795.2:n.-8+677T>C
ENST00000513189.1:c.-8+677T>C ENSP00000423386.1:n.-8+677T>C
NM_003265.2:c.-8+677T>C , LRG_117t1:c.-8+677T>C NP_003256.1:n.-8+677T>C
NM_003265.3:c.-8+677T>C MANE Select NP_003256.1:n.-8+677T>C