Canonical Allele Identifier: CA334645884
Gene:
MyVariant.info:
GRCh38 chrX:g.114583809G>A
GRCh37 chrX:g.113818282G>A
gnomAD v2:
X:113818282 G / A
gnomAD v3:
X:114583809 G / A
gnomAD v4:
chrX-114583809-G-A
Joint Max Group AF 0.26078179 (SAS)
Genomes Max Group AF 0.26078179 (SAS)
ClinVar RCV:
RCV001753216
ClinVar Variation:
1318441
dbSNP:
3813928
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.114583809G>A , CM000685.2:g.114583809G>A GRCh38
NC_000023.10:g.113818282G>A , CM000685.1:g.113818282G>A GRCh37
NC_000023.9:g.113724538G>A NCBI36
NG_012082.2:g.4725G>A
NG_012082.3:g.4725G>A
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