ClinGen Allele Registry
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Canonical Allele Identifier:
CA10902387
Gene:
Linked Data - Expert Curation
COSMIC:
COSN6462492 (not active)
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.59928177A>C
GRCh37
chr1:g.60393849A>C
Linked Data - Sequence & Population
gnomAD v2:
1:60393849 A / C
gnomAD v3:
1:59928177 A / C
gnomAD v4:
chr1-59928177-A-C
Joint Max Group AF
0.16442666 (AMR)
Genomes Max Group AF
0.16442666 (AMR)
Linked Data - NCBI & NCI
dbSNP:
11572182
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.59928177A>C , CM000663.2:g.59928177A>C
GRCh38
NC_000001.10:g.60393849A>C , CM000663.1:g.60393849A>C
GRCh37
NC_000001.9:g.60166437A>C
NCBI36
NG_007931.1:g.3575T>G
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