Canonical Allele Identifier: CA1504533026
Gene: TLR2 HGNC NCBI

Linked Data

dbSNP Id: rs1735501502
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.153684221G>A , CM000666.2:g.153684221G>A GRCh38
NC_000004.11:g.154605373G>A , CM000666.1:g.154605373G>A GRCh37
NC_000004.10:g.154824823G>A NCBI36
NG_016229.1:g.4933G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000646900.2:c.-287G>A ENSP00000493968.2:n.-287G>A
ENST00000646900.1:c.-287G>A ENSP00000493968.1:n.-287G>A
XM_017008573.1:c.-586G>A XP_016864062.1:n.-586G>A
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