Canonical Allele Identifier: CA74732809
Gene: TLR9 HGNC NCBI

Linked Data

dbSNP Id: rs955435380
MyVariant Identifiers: chr3:g.52258235G>A (hg19) chr3:g.52224219G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52224219G>A , CM000665.2:g.52224219G>A GRCh38
NC_000003.11:g.52258235G>A , CM000665.1:g.52258235G>A GRCh37
NC_000003.10:g.52233275G>A NCBI36
NG_033933.1:g.6945C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360658.3:c.97C>T MANE Select ENSP00000353874.2:p.Leu33=
ENST00000360658.2:c.97C>T ENSP00000353874.2:p.Leu33=
ENST00000478201.1:c.271C>T
ENST00000494383.1:c.557C>T
NM_017442.3:c.97C>T NP_059138.1:p.Leu33=
NM_017442.4:c.97C>T MANE Select NP_059138.1:p.Leu33=
Search 100 bp 5'
Search 100 bp 3'