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Canonical Allele Identifier:
CA14071005
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.92757645C>T
GRCh37
chr14:g.93223990C>T
Linked Data - Sequence & Population
gnomAD v2:
14:93223990 C / T
gnomAD v3:
14:92757645 C / T
gnomAD v4:
chr14-92757645-C-T
Joint Max Group AF
0.45244544 (EAS)
Genomes Max Group AF
0.45244544 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7160685
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.92757645C>T , CM000676.2:g.92757645C>T
GRCh38
NC_000014.8:g.93223990C>T , CM000676.1:g.93223990C>T
GRCh37
NC_000014.7:g.92293743C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'