Canonical Allele Identifier: CA891863013
Gene: TLR8-AS1 HGNC NCBI
ClinVar RCV:
RCV000722145
ClinVar Variation:
590975
dbSNP:
1569113445
MyVariant.info:
GRCh38 chrX:g.12906527G>C
GRCh37 chrX:g.12924646G>C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.12906527G>C , CM000685.2:g.12906527G>C GRCh38
NC_000023.10:g.12924646G>C , CM000685.1:g.12924646G>C GRCh37
NC_000023.9:g.12834567G>C NCBI36
NG_012882.2:g.4908G>C

Transcript Alleles

HGVS Amino-acid Change
NR_030727.1:n.359-276C>G
Search 100 bp 5'
Search 100 bp 3'