Canonical Allele Identifier: CA108709086

Gene: TLR2

Linked Data

• dbSNP Id: rs11938228
• gnomAD v2: 4-154621946-C-T
• gnomAD v3: 4-153700794-C-T
• gnomAD v4: 4-153700794-C-T
• MyVariant Identifiers: chr4:g.154621946C>T (hg19) ; chr4:g.153700794C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.153700794C>T , CM000666.2:g.153700794C>T	GRCh38
NC_000004.11:g.154621946C>T , CM000666.1:g.154621946C>T	GRCh37
NC_000004.10:g.154841396C>T	NCBI36
NG_016229.1:g.21506C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000643501.2:c.-300-1433C>T	ENSP00000496208.2:n.-300-1433C>T
ENST00000646219.2:c.-300-1433C>T	ENSP00000496676.2:n.-300-1433C>T
ENST00000646900.2:c.-16-2098C>T	ENSP00000493968.2:n.-16-2098C>T
ENST00000642580.1:c.-16-2098C>T	ENSP00000495339.1:n.-16-2098C>T
ENST00000642700.2:c.-16-2098C>T MANE Select	ENSP00000494425.1:n.-16-2098C>T
ENST00000643501.1:c.-300-1433C>T	ENSP00000496208.1:n.-300-1433C>T
ENST00000646219.1:c.-300-1433C>T	ENSP00000496676.1:n.-300-1433C>T
ENST00000646900.1:c.-16-2098C>T	ENSP00000493968.1:n.-16-2098C>T
NM_003264.3:c.-16-2098C>T	NP_003255.2:n.-16-2098C>T
XM_005263194.2:c.-16-2098C>T	XP_005263251.1:n.-16-2098C>T
XM_005263195.2:c.-16-2098C>T	XP_005263252.1:n.-16-2098C>T
XM_005263196.2:c.-16-2098C>T	XP_005263253.1:n.-16-2098C>T
XM_005263197.2:c.-16-2098C>T	XP_005263254.1:n.-16-2098C>T
XM_011532215.1:c.-16-2098C>T	XP_011530517.1:n.-16-2098C>T
XM_011532216.1:c.-16-2098C>T	XP_011530518.1:n.-16-2098C>T
NM_001318787.1:c.-300-1433C>T	NP_001305716.1:n.-300-1433C>T
NM_001318789.1:c.-16-2098C>T	NP_001305718.1:n.-16-2098C>T
NM_001318790.1:c.-16-2098C>T	NP_001305719.1:n.-16-2098C>T
NM_001318791.1:c.-16-2098C>T	NP_001305720.1:n.-16-2098C>T
NM_001318793.1:c.-16-2098C>T	NP_001305722.1:n.-16-2098C>T
NM_001318795.1:c.-16-2098C>T	NP_001305724.1:n.-16-2098C>T
NM_001318796.1:c.-16-2098C>T	NP_001305725.1:n.-16-2098C>T
NM_003264.4:c.-16-2098C>T	NP_003255.2:n.-16-2098C>T
XM_011532215.2:c.-16-2098C>T	XP_011530517.1:n.-16-2098C>T
XM_011532216.2:c.-16-2098C>T	XP_011530518.1:n.-16-2098C>T
XM_017008573.1:c.-300-1433C>T	XP_016864062.1:n.-300-1433C>T
XM_017008574.1:c.-151-1582C>T	XP_016864063.1:n.-151-1582C>T
XM_017008575.1:c.-16-2098C>T	XP_016864064.1:n.-16-2098C>T
NM_001318787.2:c.-300-1433C>T	NP_001305716.1:n.-300-1433C>T
NM_001318789.2:c.-16-2098C>T MANE Select	NP_001305718.1:n.-16-2098C>T
NM_001318790.2:c.-16-2098C>T	NP_001305719.1:n.-16-2098C>T
NM_001318791.2:c.-16-2098C>T	NP_001305720.1:n.-16-2098C>T
NM_001318793.2:c.-16-2098C>T	NP_001305722.1:n.-16-2098C>T
NM_001318795.2:c.-16-2098C>T	NP_001305724.1:n.-16-2098C>T
NM_001318796.2:c.-16-2098C>T	NP_001305725.1:n.-16-2098C>T
NM_003264.5:c.-16-2098C>T	NP_003255.2:n.-16-2098C>T