Canonical Allele Identifier: CA337740470
Gene: ANOS2P HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.13887364G>A
GRCh37 chrY:g.15999244G>A
gnomAD v3:
Y:13887364 G / A
gnomAD v4:
chrY-13887364-G-A
Joint Max Group AF 0.10998565 (EAS)
Genomes Max Group AF 0.13808994 (EAS)
Exomes Max Group AF 0.10412352 (EAS)
dbSNP:
34893929
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13887364G>A , CM000686.2:g.13887364G>A GRCh38
NC_000024.9:g.15999244G>A , CM000686.1:g.15999244G>A GRCh37
NC_000024.8:g.14508638G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000652544.1:n.1303G>A
ENST00000472227.5:n.1029G>A
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