Canonical Allele Identifier: CA640270919

Gene:

Linked Data

• dbSNP Id: rs1189974403
• gnomAD v2: X-990201-G-T
• gnomAD v3: X-1029466-G-T
• gnomAD v4: X-1029466-G-T
• MyVariant Identifiers: chrX:g.990201G>T (hg19) ; chrX:g.1029466G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.1029466G>T , CM000685.2:g.1029466G>T	GRCh38
NC_000023.10:g.990201G>T , CM000685.1:g.990201G>T	GRCh37
NC_000023.9:g.910201G>T	NCBI36