Canonical Allele Identifier: CA1364757122
Gene: TLR9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52224275A= , CM000665.2:g.52224275A= GRCh38
NC_000003.11:g.52258291A= , CM000665.1:g.52258291A= GRCh37
NC_000003.10:g.52233331A= NCBI36
NG_033933.1:g.6889T=

Transcript Alleles

HGVS Amino-acid change
ENST00000360658.3:c.41T= MANE Select ENSP00000353874.2:p.Leu14=
ENST00000360658.2:c.41T= ENSP00000353874.2:p.Leu14=
ENST00000478201.1:c.223-8T=
ENST00000494383.1:c.501T=
NM_017442.3:c.41T= NP_059138.1:p.Leu14=
NM_017442.4:c.41T= MANE Select NP_059138.1:p.Leu14=