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Canonical Allele Identifier:
CA13968878
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.92297047G>T
GRCh37
chr14:g.92763391G>T
Linked Data - Sequence & Population
gnomAD v2:
14:92763391 G / T
gnomAD v3:
14:92297047 G / T
gnomAD v4:
chr14-92297047-G-T
Joint Max Group AF
0.43797176 (NFE)
Genomes Max Group AF
0.43797176 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4900109
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.92297047G>T , CM000676.2:g.92297047G>T
GRCh38
NC_000014.8:g.92763391G>T , CM000676.1:g.92763391G>T
GRCh37
NC_000014.7:g.91833144G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'