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Canonical Allele Identifier:
CA13994472
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.68787474C>T
GRCh37
chr14:g.69254191C>T
Linked Data - Sequence & Population
gnomAD v2:
14:69254191 C / T
gnomAD v3:
14:68787474 C / T
gnomAD v4:
chr14-68787474-C-T
Joint Max Group AF
0.65164964 (EAS)
Genomes Max Group AF
0.65164964 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4902647
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.68787474C>T , CM000676.2:g.68787474C>T
GRCh38
NC_000014.8:g.69254191C>T , CM000676.1:g.69254191C>T
GRCh37
NC_000014.7:g.68323944C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'