ClinGen Allele Registry
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Canonical Allele Identifier:
CA14282611
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.51296620G>A
GRCh37
chr16:g.51330531G>A
Linked Data - Sequence & Population
gnomAD v2:
16:51330531 G / A
gnomAD v3:
16:51296620 G / A
gnomAD v4:
chr16-51296620-G-A
Joint Max Group AF
0.6996684 (EAS)
Genomes Max Group AF
0.6996684 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4131099
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.51296620G>A , CM000678.2:g.51296620G>A
GRCh38
NC_000016.9:g.51330531G>A , CM000678.1:g.51330531G>A
GRCh37
NC_000016.8:g.49888032G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'