ClinGen Allele Registry
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Canonical Allele Identifier:
CA14617729
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.62321458G>A
GRCh37
chr18:g.59988691G>A
Linked Data - Sequence & Population
gnomAD v2:
18:59988691 G / A
gnomAD v3:
18:62321458 G / A
gnomAD v4:
chr18-62321458-G-A
Joint Max Group AF
0.36679307 (AFR)
Genomes Max Group AF
0.36679307 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7226991
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.62321458G>A , CM000680.2:g.62321458G>A
GRCh38
NC_000018.9:g.59988691G>A , CM000680.1:g.59988691G>A
GRCh37
NC_000018.8:g.58139671G>A
NCBI36
NG_008098.1:g.1144G>A , LRG_194:g.1144G>A
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