ClinGen Allele Registry
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Canonical Allele Identifier:
CA281515969
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.56960324A>C
GRCh37
chr16:g.56994236A>C
Linked Data - Sequence & Population
gnomAD v2:
16:56994236 A / C
gnomAD v3:
16:56960324 A / C
gnomAD v4:
chr16-56960324-A-C
Joint Max Group AF
0.00068161 (AFR)
Genomes Max Group AF
0.00068161 (AFR)
Linked Data - NCBI & NCI
dbSNP:
36229492
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.56960324A>C , CM000678.2:g.56960324A>C
GRCh38
NC_000016.9:g.56994236A>C , CM000678.1:g.56994236A>C
GRCh37
NC_000016.8:g.55551737A>C
NCBI36
NG_008952.1:g.3402A>C
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