ClinGen Allele Registry
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Canonical Allele Identifier:
CA15876239
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.69727660C>T
GRCh37
chr16:g.69761563C>T
Linked Data - Sequence & Population
gnomAD v2:
16:69761563 C / T
gnomAD v3:
16:69727660 C / T
gnomAD v4:
chr16-69727660-C-T
Joint Max Group AF
0.90524292 (AMR)
Genomes Max Group AF
0.90524292 (AMR)
Linked Data - NCBI & NCI
dbSNP:
689456
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.69727660C>T , CM000678.2:g.69727660C>T
GRCh38
NC_000016.9:g.69761563C>T , CM000678.1:g.69761563C>T
GRCh37
NC_000016.8:g.68319064C>T
NCBI36
NG_011504.1:g.3971G>A
NG_011504.2:g.3971G>A
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