ClinGen Allele Registry
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Canonical Allele Identifier:
CA15694378
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.116793324G>A
GRCh37
chr11:g.116664040G>A
Linked Data - Sequence & Population
gnomAD v2:
11:116664040 G / A
gnomAD v3:
11:116793324 G / A
gnomAD v4:
chr11-116793324-G-A
Joint Max Group AF
0.78607808 (NFE)
Genomes Max Group AF
0.78607808 (NFE)
Linked Data - NCBI & NCI
dbSNP:
10750097
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.116793324G>A , CM000673.2:g.116793324G>A
GRCh38
NC_000011.9:g.116664040G>A , CM000673.1:g.116664040G>A
GRCh37
NC_000011.8:g.116169250G>A
NCBI36
NG_015894.1:g.4097C>T
NG_015894.2:g.4097C>T
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