ClinGen Allele Registry
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Canonical Allele Identifier:
CA14066071
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr14:g.94375029A>G
GRCh37
chr14:g.94841366A>G
Linked Data - Sequence & Population
gnomAD v2:
14:94841366 A / G
gnomAD v3:
14:94375029 A / G
gnomAD v4:
chr14-94375029-A-G
Joint Max Group AF
0.94854904 (AFR)
Genomes Max Group AF
0.94854904 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1243168
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.94375029A>G , CM000676.2:g.94375029A>G
GRCh38
NC_000014.8:g.94841366A>G , CM000676.1:g.94841366A>G
GRCh37
NC_000014.7:g.93911119A>G
NCBI36
NG_008290.1:g.20664T>C
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