ClinGen Allele Registry
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Canonical Allele Identifier:
CA622339237
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.56960228C>A
GRCh37
chr16:g.56994140C>A
Linked Data - Sequence & Population
gnomAD v2:
16:56994140 C / A
gnomAD v3:
16:56960228 C / A
gnomAD v4:
chr16-56960228-C-A
Joint Max Group AF
0.00004742 (AFR)
Genomes Max Group AF
0.00004742 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1157327991
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.56960228C>A , CM000678.2:g.56960228C>A
GRCh38
NC_000016.9:g.56994140C>A , CM000678.1:g.56994140C>A
GRCh37
NC_000016.8:g.55551641C>A
NCBI36
NG_008952.1:g.3306C>A
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