Canonical Allele Identifier: CA433881973
Gene: TLR9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.52258296A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52224280A>G , CM000665.2:g.52224280A>G GRCh38
NC_000003.11:g.52258296A>G , CM000665.1:g.52258296A>G GRCh37
NC_000003.10:g.52233336A>G NCBI36
NG_033933.1:g.6884T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360658.3:c.36T>C MANE Select ENSP00000353874.2:p.Ser12=
ENST00000360658.2:c.36T>C ENSP00000353874.2:p.Ser12=
ENST00000478201.1:c.223-13T>C
ENST00000494383.1:c.496T>C
NM_017442.3:c.36T>C NP_059138.1:p.Ser12=
NM_017442.4:c.36T>C MANE Select NP_059138.1:p.Ser12=
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