ClinGen Allele Registry
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Canonical Allele Identifier:
CA14530595
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.13916388A>G
GRCh37
chr18:g.13916387A>G
Linked Data - Sequence & Population
gnomAD v2:
18:13916387 A / G
gnomAD v3:
18:13916388 A / G
gnomAD v4:
chr18-13916388-A-G
Joint Max Group AF
0.67534842 (AFR)
Genomes Max Group AF
0.67534842 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1893219
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.13916388A>G , CM000680.2:g.13916388A>G
GRCh38
NC_000018.9:g.13916387A>G , CM000680.1:g.13916387A>G
GRCh37
NC_000018.8:g.13906387A>G
NCBI36
NG_011819.1:g.4149T>C
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