Canonical Allele Identifier: CA433881803
Gene: TLR9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.52258173C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52224157C>A , CM000665.2:g.52224157C>A GRCh38
NC_000003.11:g.52258173C>A , CM000665.1:g.52258173C>A GRCh37
NC_000003.10:g.52233213C>A NCBI36
NG_033933.1:g.7007G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360658.3:c.159G>T MANE Select ENSP00000353874.2:p.Val53=
ENST00000360658.2:c.159G>T ENSP00000353874.2:p.Val53=
ENST00000478201.1:c.333G>T
ENST00000494383.1:c.619G>T
NM_017442.3:c.159G>T NP_059138.1:p.Val53=
NM_017442.4:c.159G>T MANE Select NP_059138.1:p.Val53=