Canonical Allele Identifier: CA543055904

Gene: TLR9

Linked Data

• dbSNP Id: rs1333438179
• gnomAD v2: 3-52258371-C-CT
• gnomAD v4: 3-52224355-C-CT
• MyVariant Identifiers: chr3:g.52258371_52258372insT (hg19) ; chr3:g.52224355_52224356insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52224356dup , CM000665.2:g.52224356dup	GRCh38
NC_000003.11:g.52258372dup , CM000665.1:g.52258372dup	GRCh37
NC_000003.10:g.52233412dup	NCBI36
NG_033933.1:g.6808dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000360658.3:c.4-44dup MANE Select	ENSP00000353874.2:n.4-44dup
ENST00000360658.2:c.4-44dup	ENSP00000353874.2:n.4-44dup
ENST00000478201.1:c.223-89dup
ENST00000494383.1:c.464-44dup
NM_017442.3:c.4-44dup	NP_059138.1:n.4-44dup
NM_017442.4:c.4-44dup MANE Select	NP_059138.1:n.4-44dup