Canonical Allele Identifier: CA353105621
Gene: TLR9 HGNC NCBI

Linked Data

dbSNP Id: rs1699598705
gnomAD v4: 3-52224282-A-G
MyVariant Identifiers: chr3:g.52258298A>G (hg19) chr3:g.52224282A>G (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000360658.3:c.34T>C MANE Select ENSP00000353874.2:p.Ser12Pro
ENST00000360658.2:c.34T>C ENSP00000353874.2:p.Ser12Pro
ENST00000478201.1:c.223-15T>C
ENST00000494383.1:c.494T>C
NM_017442.3:c.34T>C NP_059138.1:p.Ser12Pro
NM_017442.4:c.34T>C MANE Select NP_059138.1:p.Ser12Pro
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