Canonical Allele Identifier: CA11914362
Gene: TLR3 HGNC NCBI
MyVariant.info:
GRCh38 chr4:g.186079102C>T
GRCh37 chr4:g.187000256C>T
gnomAD v2:
4:187000256 C / T
gnomAD v3:
4:186079102 C / T
gnomAD v4:
chr4-186079102-C-T
Joint Max Group AF 0.24552876 (EAS)
Genomes Max Group AF 0.23189335 (EAS)
Exomes Max Group AF 0.24618737 (EAS)
dbSNP:
5743312
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186079102C>T , CM000666.2:g.186079102C>T GRCh38
NC_000004.11:g.187000256C>T , CM000666.1:g.187000256C>T GRCh37
NC_000004.10:g.187237250C>T NCBI36
NG_007278.1:g.14948C>T , LRG_117:g.14948C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698351.1:c.633+71C>T ENSP00000513674.1:n.633+71C>T
ENST00000698352.1:c.*185+71C>T ENSP00000513675.1:n.*185+71C>T
ENST00000296795.8:c.633+71C>T MANE Select ENSP00000296795.3:n.633+71C>T
ENST00000296795.7:c.633+71C>T ENSP00000296795.2:n.633+71C>T
ENST00000513189.1:c.633+71C>T ENSP00000423386.1:n.633+71C>T
NM_003265.2:c.633+71C>T , LRG_117t1:c.633+71C>T NP_003256.1:n.633+71C>T
NM_003265.3:c.633+71C>T MANE Select NP_003256.1:n.633+71C>T
Search 100 bp 5'
Search 100 bp 3'