ClinGen Allele Registry
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Canonical Allele Identifier:
CA15882919
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr16:g.69554669T>C
GRCh37
chr16:g.69588572T>C
Linked Data - Sequence & Population
gnomAD v2:
16:69588572 T / C
gnomAD v3:
16:69554669 T / C
gnomAD v4:
chr16-69554669-T-C
Joint Max Group AF
0.41449535 (NFE)
Genomes Max Group AF
0.41449535 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1364063
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.69554669T>C , CM000678.2:g.69554669T>C
GRCh38
NC_000016.9:g.69588572T>C , CM000678.1:g.69588572T>C
GRCh37
NC_000016.8:g.68146073T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'