Canonical Allele Identifier: CA792327401
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1330139814
MyVariant Identifiers: chr4:g.187000407C>A (hg19) chr4:g.186079253C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186079253C>A , CM000666.2:g.186079253C>A GRCh38
NC_000004.11:g.187000407C>A , CM000666.1:g.187000407C>A GRCh37
NC_000004.10:g.187237401C>A NCBI36
NG_007278.1:g.15099C>A , LRG_117:g.15099C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698351.1:c.633+222C>A ENSP00000513674.1:n.633+222C>A
ENST00000698352.1:c.*185+222C>A ENSP00000513675.1:n.*185+222C>A
ENST00000296795.8:c.633+222C>A MANE Select ENSP00000296795.3:n.633+222C>A
ENST00000296795.7:c.633+222C>A ENSP00000296795.2:n.633+222C>A
ENST00000513189.1:c.633+222C>A ENSP00000423386.1:n.633+222C>A
NM_003265.2:c.633+222C>A , LRG_117t1:c.633+222C>A NP_003256.1:n.633+222C>A
NM_003265.3:c.633+222C>A MANE Select NP_003256.1:n.633+222C>A
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