Canonical Allele Identifier: CA334701378

Gene:

Linked Data

• dbSNP Id: rs907422239
• MyVariant Identifiers: chrX:g.115688192C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.115688192C>T , CM000685.2:g.115688192C>T	GRCh38
NC_000023.10:g.114922512C>T , CM000685.1:g.114922512C>T	GRCh37
NC_000023.9:g.114828768C>T	NCBI36