Canonical Allele Identifier: CA337382708
Gene:

Linked Data

dbSNP Id: rs73616508
MyVariant Identifiers: chrY:g.10151776A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.10151776A>G , CM000686.2:g.10151776A>G GRCh38