Canonical Allele Identifier: CA337740815
Gene: ANOS2P HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.13907192G>C
GRCh37 chrY:g.16019072G>C
gnomAD v3:
Y:13907192 G / C
gnomAD v4:
chrY-13907192-G-C
Joint Max Group AF 0.02194424 (MID)
Genomes Max Group AF 0.0115225 (AMR)
Exomes Max Group AF 0.02496145 (MID)
dbSNP:
34179999
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13907192G>C , CM000686.2:g.13907192G>C GRCh38
NC_000024.9:g.16019072G>C , CM000686.1:g.16019072G>C GRCh37
NC_000024.8:g.14528466G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000472227.5:n.1615+146G>C
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