ClinGen Allele Registry
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Canonical Allele Identifier:
CA14290942
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.89600929T>C
GRCh37
chr16:g.89667337T>C
Linked Data - Sequence & Population
gnomAD v2:
16:89667337 T / C
gnomAD v3:
16:89600929 T / C
gnomAD v4:
chr16-89600929-T-C
Joint Max Group AF
0.49053976 (AFR)
Genomes Max Group AF
0.49053976 (AFR)
Linked Data - NCBI & NCI
dbSNP:
154659
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.89600929T>C , CM000678.2:g.89600929T>C
GRCh38
NC_000016.9:g.89667337T>C , CM000678.1:g.89667337T>C
GRCh37
NC_000016.8:g.88194838T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'