Canonical Allele Identifier: CA353105532
Gene: TLR9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.52258289C>A (hg19) chr3:g.52224273C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52224273C>A , CM000665.2:g.52224273C>A GRCh38
NC_000003.11:g.52258289C>A , CM000665.1:g.52258289C>A GRCh37
NC_000003.10:g.52233329C>A NCBI36
NG_033933.1:g.6891G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360658.3:c.43G>T MANE Select ENSP00000353874.2:p.Val15Leu
ENST00000360658.2:c.43G>T ENSP00000353874.2:p.Val15Leu
ENST00000478201.1:c.223-6G>T
ENST00000494383.1:c.503G>T
NM_017442.3:c.43G>T NP_059138.1:p.Val15Leu
NM_017442.4:c.43G>T MANE Select NP_059138.1:p.Val15Leu
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Search 100 bp 3'