ClinGen Allele Registry
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Canonical Allele Identifier:
CA622338787
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.56957465G>A
GRCh37
chr16:g.56991377G>A
Linked Data - Sequence & Population
gnomAD v2:
16:56991377 G / A
gnomAD v3:
16:56957465 G / A
gnomAD v4:
chr16-56957465-G-A
Joint Max Group AF
0.00026289 (EAS)
Genomes Max Group AF
0.00026289 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1385369790
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.56957465G>A , CM000678.2:g.56957465G>A
GRCh38
NC_000016.9:g.56991377G>A , CM000678.1:g.56991377G>A
GRCh37
NC_000016.8:g.55548878G>A
NCBI36
NG_008952.1:g.543G>A
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