ClinGen Allele Registry
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Canonical Allele Identifier:
CA622338788
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.56957481A>G
GRCh37
chr16:g.56991393A>G
Linked Data - Sequence & Population
gnomAD v2:
16:56991393 A / G
gnomAD v3:
16:56957481 A / G
gnomAD v4:
chr16-56957481-A-G
Joint Max Group AF
0.00001919 (AFR)
Genomes Max Group AF
0.00001919 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1413905271
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.56957481A>G , CM000678.2:g.56957481A>G
GRCh38
NC_000016.9:g.56991393A>G , CM000678.1:g.56991393A>G
GRCh37
NC_000016.8:g.55548894A>G
NCBI36
NG_008952.1:g.559A>G
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