Canonical Allele Identifier: CA326797293
Gene: TLR7 HGNC NCBI

Linked Data

dbSNP Id: rs3853839
gnomAD v2: X-12907658-C-G
gnomAD v3: X-12889539-C-G
gnomAD v4: X-12889539-C-G
MyVariant Identifiers: chrX:g.12907658C>G (hg19) chrX:g.12889539C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.12889539C>G , CM000685.2:g.12889539C>G GRCh38
NC_000023.10:g.12907658C>G , CM000685.1:g.12907658C>G GRCh37
NC_000023.9:g.12817579C>G NCBI36
NG_012569.1:g.27457C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000380659.4:c.*881C>G MANE Select ENSP00000370034.3:n.*881C>G
ENST00000380659.3:c.*881C>G ENSP00000370034.3:n.*881C>G
NM_016562.3:c.*881C>G NP_057646.1:n.*881C>G
NM_016562.4:c.*881C>G MANE Select NP_057646.1:n.*881C>G
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