ClinGen Allele Registry
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Canonical Allele Identifier:
CA337217731
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.16555635G>C
GRCh37
chrY:g.18667515G>C
Linked Data - Sequence & Population
gnomAD v3:
Y:16555635 G / C
gnomAD v4:
chrY-16555635-G-C
Joint Max Group AF
0.00185616 (AFR)
Genomes Max Group AF
0.00185616 (AFR)
Linked Data - NCBI & NCI
dbSNP:
111990900
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.16555635G>C , CM000686.2:g.16555635G>C
GRCh38
NC_000024.9:g.18667515G>C , CM000686.1:g.18667515G>C
GRCh37
NC_000024.8:g.17176909G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'