Canonical Allele Identifier: CA337382664
Gene:

Linked Data

dbSNP Id: rs998815369
MyVariant Identifiers: chrY:g.10151744C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.10151744C>T , CM000686.2:g.10151744C>T GRCh38
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