Canonical Allele Identifier: CA74732879

Gene: TLR9

Linked Data

• dbSNP Id: rs888815556
• gnomAD v2: 3-52258383-A-G
• gnomAD v3: 3-52224367-A-G
• gnomAD v4: 3-52224367-A-G
• MyVariant Identifiers: chr3:g.52258383A>G (hg19) ; chr3:g.52224367A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52224367A>G , CM000665.2:g.52224367A>G	GRCh38
NC_000003.11:g.52258383A>G , CM000665.1:g.52258383A>G	GRCh37
NC_000003.10:g.52233423A>G	NCBI36
NG_033933.1:g.6797T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360658.3:c.4-55T>C MANE Select	ENSP00000353874.2:n.4-55T>C
ENST00000360658.2:c.4-55T>C	ENSP00000353874.2:n.4-55T>C
ENST00000478201.1:c.223-100T>C
ENST00000494383.1:c.464-55T>C
NM_017442.3:c.4-55T>C	NP_059138.1:n.4-55T>C
NM_017442.4:c.4-55T>C MANE Select	NP_059138.1:n.4-55T>C