Canonical Allele Identifier: CA11685813
Gene: TLR1 HGNC NCBI
dbSNP:
17616434
gnomAD v2:
4:38812876 T / C
gnomAD v3:
4:38811255 T / C
gnomAD v4:
chr4-38811255-T-C
Joint Max Group AF 0.7899107 (AFR)
Genomes Max Group AF 0.7899107 (AFR)
MyVariant.info:
GRCh38 chr4:g.38811255T>C
GRCh37 chr4:g.38812876T>C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.38811255T>C , CM000666.2:g.38811255T>C GRCh38
NC_000004.11:g.38812876T>C , CM000666.1:g.38812876T>C GRCh37
NC_000004.10:g.38489271T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000506146.5:c.-352-6062A>G ENSP00000423725.1:n.-352-6062A>G
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