Canonical Allele Identifier: CA333122058

Gene:

Linked Data

• dbSNP Id: rs17556
• gnomAD v2: X-101117568-C-A
• gnomAD v3: X-101862596-C-A
• gnomAD v4: X-101862596-C-A
• MyVariant Identifiers: chrX:g.101117568C>A (hg19) ; chrX:g.101862596C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101862596C>A , CM000685.2:g.101862596C>A	GRCh38
NC_000023.10:g.101117568C>A , CM000685.1:g.101117568C>A	GRCh37
NC_000023.9:g.101004224C>A	NCBI36