Canonical Allele Identifier: CA519961512
Gene: ANOS2P HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.16018709A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13906829A>T , CM000686.2:g.13906829A>T GRCh38
NC_000024.9:g.16018709A>T , CM000686.1:g.16018709A>T GRCh37
NC_000024.8:g.14528103A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000472227.5:n.1398A>T
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