Canonical Allele Identifier: CA871319238
Gene: TLR7 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid change
ENST00000380659.4:c.*881C>T MANE Select ENSP00000370034.3:n.*881C>T
ENST00000380659.3:c.*881C>T ENSP00000370034.3:n.*881C>T
NM_016562.3:c.*881C>T NP_057646.1:n.*881C>T
NM_016562.4:c.*881C>T MANE Select NP_057646.1:n.*881C>T
Search 100 bp 5'
Search 100 bp 3'