Canonical Allele Identifier: CA433881805
Gene: TLR9 HGNC NCBI

Linked Data

dbSNP Id: rs1699597141
gnomAD v3: 3-52224157-C-T
gnomAD v4: 3-52224157-C-T
MyVariant Identifiers: chr3:g.52258173C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52224157C>T , CM000665.2:g.52224157C>T GRCh38
NC_000003.11:g.52258173C>T , CM000665.1:g.52258173C>T GRCh37
NC_000003.10:g.52233213C>T NCBI36
NG_033933.1:g.7007G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360658.3:c.159G>A MANE Select ENSP00000353874.2:p.Val53=
ENST00000360658.2:c.159G>A ENSP00000353874.2:p.Val53=
ENST00000478201.1:c.333G>A
ENST00000494383.1:c.619G>A
NM_017442.3:c.159G>A NP_059138.1:p.Val53=
NM_017442.4:c.159G>A MANE Select NP_059138.1:p.Val53=
Search 100 bp 5'
Search 100 bp 3'