Canonical Allele Identifier: CA1139347789
Gene: ANOS2P HGNC NCBI

Linked Data

dbSNP Id: rs2079820454
gnomAD v3: Y-13836570-A-G
gnomAD v4: Y-13836570-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13836570A>G , CM000686.2:g.13836570A>G GRCh38
NC_000024.9:g.15948450A>G , CM000686.1:g.15948450A>G GRCh37
NC_000024.8:g.14457844A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000652544.1:n.685-21947A>G
ENST00000430079.5:n.478-17874A>G
ENST00000460561.1:n.261-21947A>G
ENST00000472227.5:n.399-21932A>G