Canonical Allele Identifier: CA876209000
Gene:

Linked Data

dbSNP Id: rs1413479479
gnomAD v3: X-51486996-C-T
gnomAD v4: X-51486996-C-T
MyVariant Identifiers: chrX:g.51486996C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.51486996C>T , CM000685.2:g.51486996C>T GRCh38
NC_000023.10:g.51229848C>T , CM000685.1:g.51229848C>T GRCh37
NC_000023.9:g.51246588C>T NCBI36