Canonical Allele Identifier: CA95656383
Gene: TLR1 HGNC NCBI

Linked Data

dbSNP Id: rs1016904037
MyVariant Identifiers: chr4:g.38811477C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.38811477C>G , CM000666.2:g.38811477C>G GRCh38
NC_000004.11:g.38813098C>G , CM000666.1:g.38813098C>G GRCh37
NC_000004.10:g.38489493C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000506146.5:c.-352-6284G>C ENSP00000423725.1:n.-352-6284G>C