ClinGen Allele Registry
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Canonical Allele Identifier:
CA337248158
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.16795356C>A
GRCh37
chrY:g.18907236C>A
Linked Data - Sequence & Population
gnomAD v3:
Y:16795356 C / A
gnomAD v4:
chrY-16795356-C-A
Joint Max Group AF
0.9552948 (SAS)
Genomes Max Group AF
0.9552948 (SAS)
Linked Data - NCBI & NCI
dbSNP:
9786283
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.16795356C>A , CM000686.2:g.16795356C>A
GRCh38
NC_000024.9:g.18907236C>A , CM000686.1:g.18907236C>A
GRCh37
NC_000024.8:g.17416630C>A
NCBI36
Search 100 bp 5'
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