ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA337707813
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.12078566G>A
GRCh37
chrY:g.14199272G>A
Linked Data - Sequence & Population
gnomAD v3:
Y:12078566 G / A
gnomAD v4:
chrY-12078566-G-A
Joint Max Group AF
0.00218258 (SAS)
Genomes Max Group AF
0.00218258 (SAS)
Linked Data - NCBI & NCI
dbSNP:
1028462058
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.12078566G>A , CM000686.2:g.12078566G>A
GRCh38
NC_000024.9:g.14199272G>A , CM000686.1:g.14199272G>A
GRCh37
NC_000024.8:g.12709272G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'