ClinGen Allele Registry
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Canonical Allele Identifier:
CA630902887
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.77160709C>G
GRCh37
chr18:g.74872665C>G
Linked Data - Sequence & Population
gnomAD v2:
18:74872665 C / G
gnomAD v3:
18:77160709 C / G
gnomAD v4:
chr18-77160709-C-G
Joint Max Group AF
0.00000802 (AFR)
Genomes Max Group AF
0.00000802 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1812680
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.77160709C>G , CM000680.2:g.77160709C>G
GRCh38
NC_000018.9:g.74872665C>G , CM000680.1:g.74872665C>G
GRCh37
NC_000018.8:g.73001653C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'