Canonical Allele Identifier: CA874248932

Gene:

Linked Data

• dbSNP Id: rs5944185
• MyVariant Identifiers: chrX:g.25853614T>A (hg19) ; chrX:g.25835497T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.25835497T>A , CM000685.2:g.25835497T>A	GRCh38
NC_000023.10:g.25853614T>A , CM000685.1:g.25853614T>A	GRCh37
NC_000023.9:g.25763535T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001755821.2:n.470+16215T>A