Canonical Allele Identifier: CA330697238

Gene:

Linked Data

• dbSNP Id: rs904999372
• MyVariant Identifiers: chrX:g.66316162A>T (hg19) ; chrX:g.67096320A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67096320A>T , CM000685.2:g.67096320A>T	GRCh38
NC_000023.10:g.66316162A>T , CM000685.1:g.66316162A>T	GRCh37
NC_000023.9:g.66232887A>T	NCBI36