Canonical Allele Identifier: CA641829338

Gene:

Linked Data

• dbSNP Id: rs1262876339
• gnomAD v2: X-51229348-G-C
• gnomAD v3: X-51486496-G-C
• gnomAD v4: X-51486496-G-C
• MyVariant Identifiers: chrX:g.51229348G>C (hg19) ; chrX:g.51486496G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.51486496G>C , CM000685.2:g.51486496G>C	GRCh38
NC_000023.10:g.51229348G>C , CM000685.1:g.51229348G>C	GRCh37
NC_000023.9:g.51246088G>C	NCBI36