Canonical Allele Identifier: CA1139347763
Gene: ANOS2P HGNC NCBI

Linked Data

dbSNP Id: rs2079820381

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13836324del , CM000686.2:g.13836324del GRCh38
NC_000024.9:g.15948204del , CM000686.1:g.15948204del GRCh37
NC_000024.8:g.14457598del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000652544.1:n.685-22193del
ENST00000430079.5:n.478-18120del
ENST00000460561.1:n.261-22193del
ENST00000472227.5:n.399-22178del