ClinGen Allele Registry
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Canonical Allele Identifier:
CA337491189
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.20549574T>A
GRCh37
chrY:g.22711460T>A
Linked Data - Sequence & Population
gnomAD v3:
Y:20549574 T / A
gnomAD v4:
chrY-20549574-T-A
Joint Max Group AF
0.98478336 (NFE)
Genomes Max Group AF
0.98478336 (NFE)
Linked Data - NCBI & NCI
dbSNP:
9306842
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.20549574T>A , CM000686.2:g.20549574T>A
GRCh38
NC_000024.9:g.22711460T>A , CM000686.1:g.22711460T>A
GRCh37
NC_000024.8:g.21120848T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'