Canonical Allele Identifier: CA1364757128
Gene: TLR9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52224282A= , CM000665.2:g.52224282A= GRCh38
NC_000003.11:g.52258298A= , CM000665.1:g.52258298A= GRCh37
NC_000003.10:g.52233338A= NCBI36
NG_033933.1:g.6882T=

Transcript Alleles

HGVS Amino-acid change
ENST00000360658.3:c.34T= MANE Select ENSP00000353874.2:p.Ser12=
ENST00000360658.2:c.34T= ENSP00000353874.2:p.Ser12=
ENST00000478201.1:c.223-15T=
ENST00000494383.1:c.494T=
NM_017442.3:c.34T= NP_059138.1:p.Ser12=
NM_017442.4:c.34T= MANE Select NP_059138.1:p.Ser12=