Canonical Allele Identifier: CA641829328

Gene:

Linked Data

• dbSNP Id: rs1557325693
• gnomAD v2: X-51229171-T-C
• MyVariant Identifiers: chrX:g.51229171T>C (hg19) ; chrX:g.51486319T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.51486319T>C , CM000685.2:g.51486319T>C	GRCh38
NC_000023.10:g.51229171T>C , CM000685.1:g.51229171T>C	GRCh37
NC_000023.9:g.51245911T>C	NCBI36