ClinGen Allele Registry
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Canonical Allele Identifier:
CA15922305
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.72114851T>G
GRCh37
chr18:g.69782086T>G
Linked Data - Sequence & Population
gnomAD v2:
18:69782086 T / G
gnomAD v3:
18:72114851 T / G
gnomAD v4:
chr18-72114851-T-G
Joint Max Group AF
0.66420497 (NFE)
Genomes Max Group AF
0.66420497 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1550650
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.72114851T>G , CM000680.2:g.72114851T>G
GRCh38
NC_000018.9:g.69782086T>G , CM000680.1:g.69782086T>G
GRCh37
NC_000018.8:g.67933066T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'