Canonical Allele Identifier: CA337738447
Gene: ANOS2P HGNC NCBI

Linked Data

dbSNP Id: rs989852884
gnomAD v3: Y-13787196-T-A
gnomAD v4: Y-13787196-T-A
MyVariant Identifiers: chrY:g.15899076T>A (hg19) chrY:g.13787196T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13787196T>A , CM000686.2:g.13787196T>A GRCh38
NC_000024.9:g.15899076T>A , CM000686.1:g.15899076T>A GRCh37
NC_000024.8:g.14408470T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000652544.1:n.684+32407T>A
ENST00000430079.5:n.430-3723T>A
ENST00000460561.1:n.213-3723T>A
ENST00000472227.5:n.351-3723T>A
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