Canonical Allele Identifier: CA353105588
Gene: TLR9 HGNC NCBI

Linked Data

dbSNP Id: rs1288470860
gnomAD v2: 3-52258295-G-A
gnomAD v4: 3-52224279-G-A
MyVariant Identifiers: chr3:g.52258295G>A (hg19) chr3:g.52224279G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52224279G>A , CM000665.2:g.52224279G>A GRCh38
NC_000003.11:g.52258295G>A , CM000665.1:g.52258295G>A GRCh37
NC_000003.10:g.52233335G>A NCBI36
NG_033933.1:g.6885C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360658.3:c.37C>T MANE Select ENSP00000353874.2:p.Leu13Phe
ENST00000360658.2:c.37C>T ENSP00000353874.2:p.Leu13Phe
ENST00000478201.1:c.223-12C>T
ENST00000494383.1:c.497C>T
NM_017442.3:c.37C>T NP_059138.1:p.Leu13Phe
NM_017442.4:c.37C>T MANE Select NP_059138.1:p.Leu13Phe
Search 100 bp 5'
Search 100 bp 3'