Canonical Allele Identifier: CA329467848

Gene:

Linked Data

• dbSNP Id: rs908646699
• gnomAD v2: X-43614597-C-T
• gnomAD v3: X-43755350-C-T
• gnomAD v4: X-43755350-C-T
• MyVariant Identifiers: chrX:g.43614597C>T (hg19) ; chrX:g.43755350C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43755350C>T , CM000685.2:g.43755350C>T	GRCh38
NC_000023.10:g.43614597C>T , CM000685.1:g.43614597C>T	GRCh37
NC_000023.9:g.43499541C>T	NCBI36