Canonical Allele Identifier: CA326797057
Gene: TLR7 HGNC NCBI
MyVariant.info:
GRCh38 chrX:g.12885361A>T
GRCh37 chrX:g.12903480A>T
gnomAD v2:
X:12903480 A / T
gnomAD v3:
X:12885361 A / T
gnomAD v4:
chrX-12885361-A-T
Joint Max Group AF 0.00151611 (AFR)
Genomes Max Group AF 0.00152019 (AFR)
Exomes Max Group AF 0.0010934 (AFR)
dbSNP:
179009
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000380659.4:c.4-151A>T MANE Select ENSP00000370034.3:n.4-151A>T
ENST00000380659.3:c.4-151A>T ENSP00000370034.3:n.4-151A>T
NM_016562.3:c.4-151A>T NP_057646.1:n.4-151A>T
NM_016562.4:c.4-151A>T MANE Select NP_057646.1:n.4-151A>T
Search 100 bp 5'
Search 100 bp 3'