Canonical Allele Identifier: CA869981811

Gene:

Linked Data

• dbSNP Id: rs1215687106
• gnomAD v3: X-110576637-C-T
• gnomAD v4: X-110576637-C-T
• MyVariant Identifiers: chrX:g.109819865C>T (hg19) ; chrX:g.110576637C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.110576637C>T , CM000685.2:g.110576637C>T	GRCh38
NC_000023.10:g.109819865C>T , CM000685.1:g.109819865C>T	GRCh37
NC_000023.9:g.109706521C>T	NCBI36