Canonical Allele Identifier: CA337738445
Gene: ANOS2P HGNC NCBI

Linked Data

dbSNP Id: rs758044262
gnomAD v3: Y-13787185-A-T
gnomAD v4: Y-13787185-A-T
MyVariant Identifiers: chrY:g.15899065A>T (hg19) chrY:g.13787185A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13787185A>T , CM000686.2:g.13787185A>T GRCh38
NC_000024.9:g.15899065A>T , CM000686.1:g.15899065A>T GRCh37
NC_000024.8:g.14408459A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000652544.1:n.684+32396A>T
ENST00000430079.5:n.430-3734A>T
ENST00000460561.1:n.213-3734A>T
ENST00000472227.5:n.351-3734A>T
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