Canonical Allele Identifier: CA11741891

Gene: TLR3

Linked Data

• dbSNP Id: rs5743313
• gnomAD v2: 4-187000367-C-T
• gnomAD v3: 4-186079213-C-T
• gnomAD v4: 4-186079213-C-T
• MyVariant Identifiers: chr4:g.187000367C>T (hg19) ; chr4:g.187000367_187000368delinsTG (hg19) ; chr4:g.186079213C>T (hg38) ; chr4:g.186079213_186079214delinsTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186079213C>T , CM000666.2:g.186079213C>T	GRCh38
NC_000004.11:g.187000367C>T , CM000666.1:g.187000367C>T	GRCh37
NC_000004.10:g.187237361C>T	NCBI36
NG_007278.1:g.15059C>T , LRG_117:g.15059C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000698351.1:c.633+182C>T	ENSP00000513674.1:n.633+182C>T
ENST00000698352.1:c.*185+182C>T	ENSP00000513675.1:n.*185+182C>T
ENST00000296795.8:c.633+182C>T MANE Select	ENSP00000296795.3:n.633+182C>T
ENST00000296795.7:c.633+182C>T	ENSP00000296795.2:n.633+182C>T
ENST00000513189.1:c.633+182C>T	ENSP00000423386.1:n.633+182C>T
NM_003265.2:c.633+182C>T , LRG_117t1:c.633+182C>T	NP_003256.1:n.633+182C>T
NM_003265.3:c.633+182C>T MANE Select	NP_003256.1:n.633+182C>T