Canonical Allele Identifier: CA337737706
Gene: ANOS2P HGNC NCBI

Linked Data

dbSNP Id: rs113047816
gnomAD v3: Y-13750962-C-T
gnomAD v4: Y-13750962-C-T
MyVariant Identifiers: chrY:g.15862842C>T (hg19) chrY:g.13750962C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13750962C>T , CM000686.2:g.13750962C>T GRCh38
NC_000024.9:g.15862842C>T , CM000686.1:g.15862842C>T GRCh37
NC_000024.8:g.14372236C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000652544.1:n.535-3678C>T
Search 100 bp 5'
Search 100 bp 3'