Canonical Allele Identifier: CA1364757197
Gene: TLR9 HGNC NCBI

Linked Data

dbSNP Id: rs1372366710
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52224401A>C , CM000665.2:g.52224401A>C GRCh38
NC_000003.11:g.52258417A>C , CM000665.1:g.52258417A>C GRCh37
NC_000003.10:g.52233457A>C NCBI36
NG_033933.1:g.6763T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360658.3:c.4-89T>G MANE Select ENSP00000353874.2:n.4-89T>G
ENST00000360658.2:c.4-89T>G ENSP00000353874.2:n.4-89T>G
ENST00000478201.1:c.223-134T>G
ENST00000494383.1:c.464-89T>G
NM_017442.3:c.4-89T>G NP_059138.1:n.4-89T>G
NM_017442.4:c.4-89T>G MANE Select NP_059138.1:n.4-89T>G
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