Canonical Allele Identifier: CA326499300
Gene:

Linked Data

ClinVar Variation Id: 1248674
ClinVar RCV Id: RCV001654611
dbSNP Id: rs184604660
gnomAD v2: X-8700445-T-C
gnomAD v3: X-8732404-T-C
gnomAD v4: X-8732404-T-C
MyVariant Identifiers: chrX:g.8700445T>C (hg19) chrX:g.8732404T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8732404T>C , CM000685.2:g.8732404T>C GRCh38
NC_000023.10:g.8700445T>C , CM000685.1:g.8700445T>C GRCh37
NC_000023.9:g.8660445T>C NCBI36
NG_007088.1:g.4783A>G
NG_007088.2:g.4783A>G
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