Canonical Allele Identifier: CA1364757090
Gene: TLR9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52224203T= , CM000665.2:g.52224203T= GRCh38
NC_000003.11:g.52258219T= , CM000665.1:g.52258219T= GRCh37
NC_000003.10:g.52233259T= NCBI36
NG_033933.1:g.6961A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360658.3:c.113A= MANE Select ENSP00000353874.2:p.Gln38=
ENST00000360658.2:c.113A= ENSP00000353874.2:p.Gln38=
ENST00000478201.1:c.287A=
ENST00000494383.1:c.573A=
NM_017442.3:c.113A= NP_059138.1:p.Gln38=
NM_017442.4:c.113A= MANE Select NP_059138.1:p.Gln38=