Canonical Allele Identifier: CA2534170356
Gene: ANOS2P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13906782T>C , CM000686.2:g.13906782T>C GRCh38
NC_000024.9:g.16018662T>C , CM000686.1:g.16018662T>C GRCh37
NC_000024.8:g.14528056T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000472227.5:n.1395-44T>C