Canonical Allele Identifier: CA1364757119
Gene: TLR9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52224271C= , CM000665.2:g.52224271C= GRCh38
NC_000003.11:g.52258287C= , CM000665.1:g.52258287C= GRCh37
NC_000003.10:g.52233327C= NCBI36
NG_033933.1:g.6893G=

Transcript Alleles

HGVS Amino-acid change
ENST00000360658.3:c.45G= MANE Select ENSP00000353874.2:p.Val15=
ENST00000360658.2:c.45G= ENSP00000353874.2:p.Val15=
ENST00000478201.1:c.223-4G=
ENST00000494383.1:c.505G=
NM_017442.3:c.45G= NP_059138.1:p.Val15=
NM_017442.4:c.45G= MANE Select NP_059138.1:p.Val15=