Canonical Allele Identifier: CA108694509
Gene: TLR2 HGNC NCBI

Linked Data

dbSNP Id: rs912083163
gnomAD v2: 4-154605379-G-A
gnomAD v3: 4-153684227-G-A
gnomAD v4: 4-153684227-G-A
MyVariant Identifiers: chr4:g.154605379G>A (hg19) chr4:g.153684227G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.153684227G>A , CM000666.2:g.153684227G>A GRCh38
NC_000004.11:g.154605379G>A , CM000666.1:g.154605379G>A GRCh37
NC_000004.10:g.154824829G>A NCBI36
NG_016229.1:g.4939G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646900.2:c.-281G>A ENSP00000493968.2:n.-281G>A
ENST00000646900.1:c.-281G>A ENSP00000493968.1:n.-281G>A
XM_017008573.1:c.-580G>A XP_016864062.1:n.-580G>A
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