ClinGen Allele Registry
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Canonical Allele Identifier:
CA14571901
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.37636298A>G
GRCh37
chr18:g.35216261A>G
Linked Data - Sequence & Population
gnomAD v2:
18:35216261 A / G
gnomAD v3:
18:37636298 A / G
gnomAD v4:
chr18-37636298-A-G
Joint Max Group AF
0.8079003 (NFE)
Genomes Max Group AF
0.8079003 (NFE)
Linked Data - NCBI & NCI
dbSNP:
7235755
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.37636298A>G , CM000680.2:g.37636298A>G
GRCh38
NC_000018.9:g.35216261A>G , CM000680.1:g.35216261A>G
GRCh37
NC_000018.8:g.33470259A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'