Canonical Allele Identifier:
CA876208922
Gene:
MyVariant.info:
GRCh38
chrX:g.51486754G>T
gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.51486754G>T , CM000685.2:g.51486754G>T | GRCh38 |
| NC_000023.10:g.51229606G>T , CM000685.1:g.51229606G>T | GRCh37 |
| NC_000023.9:g.51246346G>T | NCBI36 |