Canonical Allele Identifier: CA74732803
Gene: TLR9 HGNC NCBI

Linked Data

dbSNP Id: rs892160452
MyVariant Identifiers: chr3:g.52258219T>A (hg19) chr3:g.52224203T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52224203T>A , CM000665.2:g.52224203T>A GRCh38
NC_000003.11:g.52258219T>A , CM000665.1:g.52258219T>A GRCh37
NC_000003.10:g.52233259T>A NCBI36
NG_033933.1:g.6961A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360658.3:c.113A>T MANE Select ENSP00000353874.2:p.Gln38Leu
ENST00000360658.2:c.113A>T ENSP00000353874.2:p.Gln38Leu
ENST00000478201.1:c.287A>T
ENST00000494383.1:c.573A>T
NM_017442.3:c.113A>T NP_059138.1:p.Gln38Leu
NM_017442.4:c.113A>T MANE Select NP_059138.1:p.Gln38Leu
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Search 100 bp 3'