Canonical Allele Identifier: CA15009634

Gene:

Linked Data

• ClinVar Variation Id: 1291836
• ClinVar RCV Id: RCV001713614
• dbSNP Id: rs56035532
• gnomAD v2: X-82763150-G-T
• gnomAD v3: X-83508142-G-T
• gnomAD v4: X-83508142-G-T
• MyVariant Identifiers: chrX:g.82763150G>T (hg19) ; chrX:g.83508142G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.83508142G>T , CM000685.2:g.83508142G>T	GRCh38
NC_000023.10:g.82763150G>T , CM000685.1:g.82763150G>T	GRCh37
NC_000023.9:g.82649806G>T	NCBI36
NG_009936.2:g.4882G>T