Canonical Allele Identifier: CA353105618
Gene: TLR9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.52258298A>T (hg19) chr3:g.52224282A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52224282A>T , CM000665.2:g.52224282A>T GRCh38
NC_000003.11:g.52258298A>T , CM000665.1:g.52258298A>T GRCh37
NC_000003.10:g.52233338A>T NCBI36
NG_033933.1:g.6882T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360658.3:c.34T>A MANE Select ENSP00000353874.2:p.Ser12Thr
ENST00000360658.2:c.34T>A ENSP00000353874.2:p.Ser12Thr
ENST00000478201.1:c.223-15T>A
ENST00000494383.1:c.494T>A
NM_017442.3:c.34T>A NP_059138.1:p.Ser12Thr
NM_017442.4:c.34T>A MANE Select NP_059138.1:p.Ser12Thr
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