Canonical Allele Identifier: CA112100701
Gene: TLR3 HGNC NCBI

Linked Data

dbSNP Id: rs568947307
gnomAD v2: 4-187006959-G-A
gnomAD v3: 4-186085805-G-A
gnomAD v4: 4-186085805-G-A
MyVariant Identifiers: chr4:g.187006959G>A (hg19) chr4:g.186085805G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186085805G>A , CM000666.2:g.186085805G>A GRCh38
NC_000004.11:g.187006959G>A , CM000666.1:g.187006959G>A GRCh37
NC_000004.10:g.187243953G>A NCBI36
NG_007278.1:g.21651G>A , LRG_117:g.21651G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698352.1:c.*3199G>A ENSP00000513675.1:n.*3199G>A
ENST00000698353.1:n.3522G>A
ENST00000698354.1:c.*932G>A ENSP00000513676.1:n.*932G>A
ENST00000296795.8:c.*932G>A MANE Select ENSP00000296795.3:n.*932G>A
ENST00000296795.7:c.*932G>A ENSP00000296795.2:n.*932G>A
NM_003265.3:c.*932G>A MANE Select NP_003256.1:n.*932G>A
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