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Canonical Allele Identifier:
CA337716053
Gene: USP9Y
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.12546187G>A
GRCh37
chrY:g.14658122G>A
Linked Data - Sequence & Population
gnomAD v3:
Y:12546187 G / A
gnomAD v4:
chrY-12546187-G-A
Joint Max Group AF
0.00039245 (AFR)
Genomes Max Group AF
0.00039245 (AFR)
Linked Data - NCBI & NCI
dbSNP:
180966744
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.12546187G>A , CM000686.2:g.12546187G>A
GRCh38
NC_000024.9:g.14658122G>A , CM000686.1:g.14658122G>A
GRCh37
NC_000024.8:g.13168132G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000457658.6:n.590G>A
Search 100 bp 5'
Search 100 bp 3'