Canonical Allele Identifier: CA198758202
Gene: TLR4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11536879

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117709933A>G , CM000671.2:g.117709933A>G GRCh38
NC_000009.11:g.120472211A>G , CM000671.1:g.120472211A>G GRCh37
NC_000009.10:g.119512032A>G NCBI36
NG_011475.1:g.10752A>G

Transcript Alleles

HGVS Amino-acid change
NM_003266.3:c.140+1204A>G VV NP_003257.1:p.=
NM_138554.4:c.260+1204A>G VV NP_612564.1:p.=
NM_138557.2:c.-340-2456A>G VV NP_612567.1:p.=
NM_138554.5:c.260+1204A>G VV MANE Preferred NP_612564.1:p.=
ENST00000355622.6:c.260+1204A>G ENSP00000363089.5:p.=
ENST00000394487.4:c.140+1204A>G ENSP00000377997.4:p.=
ENST00000472304.1:n.178-2456A>G