Canonical Allele Identifier: CA519961516
Gene: ANOS2P HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.16018710T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13906830T>A , CM000686.2:g.13906830T>A GRCh38
NC_000024.9:g.16018710T>A , CM000686.1:g.16018710T>A GRCh37
NC_000024.8:g.14528104T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000472227.5:n.1399T>A
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