Canonical Allele Identifier: CA433881919
Gene: TLR9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.52258263G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52224247G>T , CM000665.2:g.52224247G>T GRCh38
NC_000003.11:g.52258263G>T , CM000665.1:g.52258263G>T GRCh37
NC_000003.10:g.52233303G>T NCBI36
NG_033933.1:g.6917C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360658.3:c.69C>A MANE Select ENSP00000353874.2:p.Thr23=
ENST00000360658.2:c.69C>A ENSP00000353874.2:p.Thr23=
ENST00000478201.1:c.243C>A
ENST00000494383.1:c.529C>A
NM_017442.3:c.69C>A NP_059138.1:p.Thr23=
NM_017442.4:c.69C>A MANE Select NP_059138.1:p.Thr23=