Canonical Allele Identifier: CA112539828
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs537850569

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186079130C>T , CM000666.2:g.186079130C>T GRCh38
NC_000004.11:g.187000284C>T , CM000666.1:g.187000284C>T GRCh37
NC_000004.10:g.187237278C>T NCBI36
NG_007278.1:g.14976C>T , LRG_117:g.14976C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698351.1:c.633+99C>T ENSP00000513674.1:n.633+99C>T
ENST00000698352.1:c.*185+99C>T ENSP00000513675.1:n.*185+99C>T
ENST00000296795.8:c.633+99C>T MANE Select ENSP00000296795.3:n.633+99C>T
ENST00000296795.7:c.633+99C>T ENSP00000296795.2:n.633+99C>T
ENST00000513189.1:c.633+99C>T ENSP00000423386.1:n.633+99C>T
NM_003265.2:c.633+99C>T , LRG_117t1:c.633+99C>T NP_003256.1:n.633+99C>T
NM_003265.3:c.633+99C>T MANE Select NP_003256.1:n.633+99C>T