Canonical Allele Identifier:
CA876208962
Gene:
MyVariant.info:
GRCh38
chrX:g.51486867T>G
gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.51486867T>G , CM000685.2:g.51486867T>G | GRCh38 |
| NC_000023.10:g.51229719T>G , CM000685.1:g.51229719T>G | GRCh37 |
| NC_000023.9:g.51246459T>G | NCBI36 |