ClinGen Allele Registry
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Canonical Allele Identifier:
CA337737052
Gene: ANOS2P
HGNC
NCBI
Linked Data
dbSNP Id:
rs112689262
gnomAD v3:
Y-13709203-C-T
gnomAD v4:
Y-13709203-C-T
MyVariant Identifiers:
chrY:g.15821083C>T (hg19)
chrY:g.13709203C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.13709203C>T , CM000686.2:g.13709203C>T
GRCh38
NC_000024.9:g.15821083C>T , CM000686.1:g.15821083C>T
GRCh37
NC_000024.8:g.14330477C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid change
ENST00000652544.1:n.534+4768C>T
Search 100 bp 5'
Search 100 bp 3'