ClinGen Allele Registry
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Canonical Allele Identifier:
CA14299764
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.60280752G>T
GRCh37
chr16:g.60314656G>T
Linked Data - Sequence & Population
gnomAD v2:
16:60314656 G / T
gnomAD v3:
16:60280752 G / T
gnomAD v4:
chr16-60280752-G-T
Joint Max Group AF
0.1957704 (NFE)
Genomes Max Group AF
0.1957704 (NFE)
Linked Data - NCBI & NCI
dbSNP:
9932186
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.60280752G>T , CM000678.2:g.60280752G>T
GRCh38
NC_000016.9:g.60314656G>T , CM000678.1:g.60314656G>T
GRCh37
NC_000016.8:g.58872157G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'