Canonical Allele Identifier: CA337382755
Gene:

Linked Data

dbSNP Id: rs79695784
MyVariant Identifiers: chrY:g.10151805C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.10151805C>T , CM000686.2:g.10151805C>T GRCh38