Canonical Allele Identifier: CA353104470
Gene: TLR9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.52258190G>C (hg19) chr3:g.52224174G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52224174G>C , CM000665.2:g.52224174G>C GRCh38
NC_000003.11:g.52258190G>C , CM000665.1:g.52258190G>C GRCh37
NC_000003.10:g.52233230G>C NCBI36
NG_033933.1:g.6990C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360658.3:c.142C>G MANE Select ENSP00000353874.2:p.Leu48Val
ENST00000360658.2:c.142C>G ENSP00000353874.2:p.Leu48Val
ENST00000478201.1:c.316C>G
ENST00000494383.1:c.602C>G
NM_017442.3:c.142C>G NP_059138.1:p.Leu48Val
NM_017442.4:c.142C>G MANE Select NP_059138.1:p.Leu48Val
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