ClinGen Allele Registry
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Canonical Allele Identifier:
CA14359408
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.86003870C>G
GRCh37
chr16:g.86037476C>G
Linked Data - Sequence & Population
gnomAD v2:
16:86037476 C / G
gnomAD v3:
16:86003870 C / G
gnomAD v4:
chr16-86003870-C-G
Joint Max Group AF
0.26800634 (NFE)
Genomes Max Group AF
0.26800634 (NFE)
Linked Data - NCBI & NCI
dbSNP:
7197068
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.86003870C>G , CM000678.2:g.86003870C>G
GRCh38
NC_000016.9:g.86037476C>G , CM000678.1:g.86037476C>G
GRCh37
NC_000016.8:g.84594977C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'