Canonical Allele Identifier: CA337737952
Gene: ANOS2P HGNC NCBI

Linked Data

dbSNP Id: rs1033505115
MyVariant Identifiers: chrY:g.15877534G>A (hg19) chrY:g.13765654G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13765654G>A , CM000686.2:g.13765654G>A GRCh38
NC_000024.9:g.15877534G>A , CM000686.1:g.15877534G>A GRCh37
NC_000024.8:g.14386928G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000652544.1:n.684+10865G>A
ENST00000430079.5:n.429+10865G>A
ENST00000460561.1:n.212+10865G>A
ENST00000472227.5:n.350+13649G>A
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