Canonical Allele Identifier: CA10576193
Gene:
MyVariant.info:
GRCh38 chrX:g.114584047C>T
GRCh37 chrX:g.113818520C>T
gnomAD v2:
X:113818520 C / T
gnomAD v3:
X:114584047 C / T
gnomAD v4:
chrX-114584047-C-T
Joint Max Group AF 0.25294162 (SAS)
Genomes Max Group AF 0.25294162 (SAS)
Exomes Max Group AF 0.10819006 (NFE)
ClinVar RCV:
RCV001770161
ClinVar Variation:
225992
dbSNP:
3813929
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.114584047C>T , CM000685.2:g.114584047C>T GRCh38
NC_000023.10:g.113818520C>T , CM000685.1:g.113818520C>T GRCh37
NC_000023.9:g.113724776C>T NCBI36
NG_012082.2:g.4963C>T
NG_012082.3:g.4963C>T
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