Canonical Allele Identifier: CA2501477871
Gene: ANOS2P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13787144T>C , CM000686.2:g.13787144T>C GRCh38
NC_000024.9:g.15899024T>C , CM000686.1:g.15899024T>C GRCh37
NC_000024.8:g.14408418T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000652544.1:n.684+32355T>C
ENST00000430079.5:n.430-3775T>C
ENST00000460561.1:n.213-3775T>C
ENST00000472227.5:n.351-3775T>C