Canonical Allele Identifier: CA10452691

Gene: XIST

Linked Data

• ClinVar Variation Id: 3039016
• ClinVar RCV Id: RCV003914366
• dbSNP Id: rs112769630
• ExAC: X:73062455 A / G
• gnomAD v2: X-73062455-A-G
• gnomAD v3: X-73842620-A-G
• gnomAD v4: X-73842620-A-G
• MyVariant Identifiers: chrX:g.73062455A>G (hg19) ; chrX:g.73842620A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.73842620A>G , CM000685.2:g.73842620A>G	GRCh38
NC_000023.10:g.73062455A>G , CM000685.1:g.73062455A>G	GRCh37
NC_000023.9:g.72979180A>G	NCBI36
NG_016172.1:g.15134T>C

Transcript Alleles

HGVS	Amino-acid Change
NR_001564.2:n.10134T>C