ClinGen Allele Registry
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Canonical Allele Identifier:
CA337706362
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.12023887A>G
GRCh37
chrY:g.14144593A>G
Linked Data - Sequence & Population
gnomAD v3:
Y:12023887 A / G
gnomAD v4:
chrY-12023887-A-G
Joint Max Group AF
0.2802902 (MID)
Genomes Max Group AF
0.23051052 (NFE)
Linked Data - NCBI & NCI
dbSNP:
17306699
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.12023887A>G , CM000686.2:g.12023887A>G
GRCh38
NC_000024.9:g.14144593A>G , CM000686.1:g.14144593A>G
GRCh37
NC_000024.8:g.12654593A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'