Canonical Allele Identifier: CA1364757129
Gene: TLR9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52224283C= , CM000665.2:g.52224283C= GRCh38
NC_000003.11:g.52258299C= , CM000665.1:g.52258299C= GRCh37
NC_000003.10:g.52233339C= NCBI36
NG_033933.1:g.6881G=

Transcript Alleles

HGVS Amino-acid change
ENST00000360658.3:c.33G= MANE Select ENSP00000353874.2:p.Leu11=
ENST00000360658.2:c.33G= ENSP00000353874.2:p.Leu11=
ENST00000478201.1:c.223-16G=
ENST00000494383.1:c.493G=
NM_017442.3:c.33G= NP_059138.1:p.Leu11=
NM_017442.4:c.33G= MANE Select NP_059138.1:p.Leu11=