Canonical Allele Identifier: CA326797056
Gene: TLR7 HGNC NCBI
MyVariant.info:
GRCh38 chrX:g.12885361A>G
GRCh37 chrX:g.12903480A>G
gnomAD v2:
X:12903480 A / G
gnomAD v3:
X:12885361 A / G
gnomAD v4:
chrX-12885361-A-G
Joint Max Group AF 0.31089482 (AMR)
Genomes Max Group AF 0.30073466 (AMR)
Exomes Max Group AF 0.31327468 (AMR)
dbSNP:
179009
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.12885361A>G , CM000685.2:g.12885361A>G GRCh38
NC_000023.10:g.12903480A>G , CM000685.1:g.12903480A>G GRCh37
NC_000023.9:g.12813401A>G NCBI36
NG_012569.1:g.23279A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380659.4:c.4-151A>G MANE Select ENSP00000370034.3:n.4-151A>G
ENST00000380659.3:c.4-151A>G ENSP00000370034.3:n.4-151A>G
NM_016562.3:c.4-151A>G NP_057646.1:n.4-151A>G
NM_016562.4:c.4-151A>G MANE Select NP_057646.1:n.4-151A>G
Search 100 bp 5'
Search 100 bp 3'