ClinGen Allele Registry
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Canonical Allele Identifier:
CA14060799
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.48095753G>A
GRCh37
chr14:g.48564956G>A
Linked Data - Sequence & Population
gnomAD v2:
14:48564956 G / A
gnomAD v3:
14:48095753 G / A
gnomAD v4:
chr14-48095753-G-A
Joint Max Group AF
0.38207791 (AFR)
Genomes Max Group AF
0.38207791 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7151223
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.48095753G>A , CM000676.2:g.48095753G>A
GRCh38
NC_000014.8:g.48564956G>A , CM000676.1:g.48564956G>A
GRCh37
NC_000014.7:g.47634706G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'