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Canonical Allele Identifier:
CA14294709
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.11923062C>T
GRCh37
chr16:g.12016919C>T
Linked Data - Sequence & Population
gnomAD v2:
16:12016919 C / T
gnomAD v3:
16:11923062 C / T
gnomAD v4:
chr16-11923062-C-T
Joint Max Group AF
0.5775862 (NFE)
Genomes Max Group AF
0.5775862 (NFE)
Linked Data - NCBI & NCI
dbSNP:
10852344
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.11923062C>T , CM000678.2:g.11923062C>T
GRCh38
NC_000016.9:g.12016919C>T , CM000678.1:g.12016919C>T
GRCh37
NC_000016.8:g.11924420C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'