ClinGen Allele Registry
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Canonical Allele Identifier:
CA337379481
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.19247820C>G
GRCh37
chrY:g.21409706C>G
Linked Data - Sequence & Population
gnomAD v3:
Y:19247820 C / G
gnomAD v4:
chrY-19247820-C-G
Joint Max Group AF
0.9478797 (EAS)
Genomes Max Group AF
0.9478797 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4481791
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.19247820C>G , CM000686.2:g.19247820C>G
GRCh38
NC_000024.9:g.21409706C>G , CM000686.1:g.21409706C>G
GRCh37
NC_000024.8:g.19869094C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'