Canonical Allele Identifier: CA337383123
Gene:

Linked Data

dbSNP Id: rs996855987
MyVariant Identifiers: chrY:g.10152176A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.10152176A>T , CM000686.2:g.10152176A>T GRCh38