Canonical Allele Identifier:
CA337383029
Gene:
MyVariant.info:
GRCh38
chrY:g.10152056T>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.10152056T>A , CM000686.2:g.10152056T>A | GRCh38 |