Canonical Allele Identifier: CA337740810
Gene: ANOS2P HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.13906848A>G
GRCh37 chrY:g.16018728A>G
gnomAD v3:
Y:13906848 A / G
gnomAD v4:
chrY-13906848-A-G
Joint Max Group AF 0.17035626 (MID)
Genomes Max Group AF 0.07998848 (AMR)
Exomes Max Group AF 0.16484972 (MID)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13906848A>G , CM000686.2:g.13906848A>G GRCh38
NC_000024.9:g.16018728A>G , CM000686.1:g.16018728A>G GRCh37
NC_000024.8:g.14528122A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000472227.5:n.1417A>G
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