ClinGen Allele Registry
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Canonical Allele Identifier:
CA337264548
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrY:g.16926422A>C
GRCh37
chrY:g.19038302A>C
Linked Data - Sequence & Population
gnomAD v3:
Y:16926422 A / C
gnomAD v4:
chrY-16926422-A-C
Joint Max Group AF
0.25354025 (MID)
Genomes Max Group AF
0.22383459 (NFE)
Linked Data - NCBI & NCI
dbSNP:
17315772
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.16926422A>C , CM000686.2:g.16926422A>C
GRCh38
NC_000024.9:g.19038302A>C , CM000686.1:g.19038302A>C
GRCh37
NC_000024.8:g.17547696A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'