ClinGen Allele Registry
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Canonical Allele Identifier:
CA614787592
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.68787474C>A
GRCh37
chr14:g.69254191C>A
Linked Data - Sequence & Population
gnomAD v2:
14:69254191 C / A
gnomAD v3:
14:68787474 C / A
gnomAD v4:
chr14-68787474-C-A
Joint Max Group AF
0.00006837 (EAS)
Genomes Max Group AF
0.00006837 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4902647
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.68787474C>A , CM000676.2:g.68787474C>A
GRCh38
NC_000014.8:g.69254191C>A , CM000676.1:g.69254191C>A
GRCh37
NC_000014.7:g.68323944C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'