Canonical Allele Identifier: CA519961571
Gene: ANOS2P HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.16018715T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13906835T>C , CM000686.2:g.13906835T>C GRCh38
NC_000024.9:g.16018715T>C , CM000686.1:g.16018715T>C GRCh37
NC_000024.8:g.14528109T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000472227.5:n.1404T>C