Canonical Allele Identifier: CA74734719
Gene: TLR9 HGNC NCBI

Linked Data

dbSNP Id: rs1007188630
MyVariant Identifiers: chr3:g.52258415C>G (hg19) chr3:g.52224399C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52224399C>G , CM000665.2:g.52224399C>G GRCh38
NC_000003.11:g.52258415C>G , CM000665.1:g.52258415C>G GRCh37
NC_000003.10:g.52233455C>G NCBI36
NG_033933.1:g.6765G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360658.3:c.4-87G>C MANE Select ENSP00000353874.2:n.4-87G>C
ENST00000360658.2:c.4-87G>C ENSP00000353874.2:n.4-87G>C
ENST00000478201.1:c.223-132G>C
ENST00000494383.1:c.464-87G>C
NM_017442.3:c.4-87G>C NP_059138.1:n.4-87G>C
NM_017442.4:c.4-87G>C MANE Select NP_059138.1:n.4-87G>C
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