Canonical Allele Identifier: CA15000717
Gene:
MyVariant.info:
GRCh38 chrX:g.3492628A>G
GRCh37 chrX:g.3410669A>G
gnomAD v2:
X:3410669 A / G
gnomAD v3:
X:3492628 A / G
gnomAD v4:
chrX-3492628-A-G
Joint Max Group AF 0.28894967 (SAS)
Genomes Max Group AF 0.28894967 (SAS)
dbSNP:
7059886
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.3492628A>G , CM000685.2:g.3492628A>G GRCh38
NC_000023.10:g.3410669A>G , CM000685.1:g.3410669A>G GRCh37
NC_000023.9:g.3420669A>G NCBI36
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