ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA337718072
Gene: USP9Y
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.12660528T>C
GRCh37
chrY:g.14772459T>C
Linked Data - Sequence & Population
gnomAD v3:
Y:12660528 T / C
gnomAD v4:
chrY-12660528-T-C
Joint Max Group AF
0.00039049 (AFR)
Genomes Max Group AF
0.00039049 (AFR)
Linked Data - NCBI & NCI
dbSNP:
113289649
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.12660528T>C , CM000686.2:g.12660528T>C
GRCh38
NC_000024.9:g.14772459T>C , CM000686.1:g.14772459T>C
GRCh37
NC_000024.8:g.13281853T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000457658.6:n.654-1828T>C
Search 100 bp 5'
Search 100 bp 3'