ClinGen Allele Registry
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Canonical Allele Identifier:
CA14250083
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr16:g.69101146C>A
GRCh37
chr16:g.69135049C>A
Linked Data - Sequence & Population
gnomAD v2:
16:69135049 C / A
gnomAD v3:
16:69101146 C / A
gnomAD v4:
chr16-69101146-C-A
Joint Max Group AF
0.65329699 (EAS)
Genomes Max Group AF
0.65329699 (EAS)
Linked Data - NCBI & NCI
dbSNP:
8047014
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.69101146C>A , CM000678.2:g.69101146C>A
GRCh38
NC_000016.9:g.69135049C>A , CM000678.1:g.69135049C>A
GRCh37
NC_000016.8:g.67692550C>A
NCBI36
NG_047056.1:g.583C>A
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