Canonical Allele Identifier: CA11712170
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs10025405

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085652A>G , CM000666.2:g.186085652A>G GRCh38
NC_000004.11:g.187006806A>G , CM000666.1:g.187006806A>G GRCh37
NC_000004.10:g.187243800A>G NCBI36
NG_007278.1:g.21498A>G , LRG_117:g.21498A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000296795.8:c.*779A>G MANE Select ENSP00000296795.3:p.=
ENST00000296795.7:c.*779A>G ENSP00000296795.2:p.=
NM_003265.3:c.*779A>G MANE Select NP_003256.1:p.=