Canonical Allele Identifier:
CA876208968
Gene:
MyVariant.info:
GRCh38
chrX:g.51486885C>A
gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.51486885C>A , CM000685.2:g.51486885C>A | GRCh38 |
| NC_000023.10:g.51229737C>A , CM000685.1:g.51229737C>A | GRCh37 |
| NC_000023.9:g.51246477C>A | NCBI36 |