ClinGen Allele Registry
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Canonical Allele Identifier:
CA297891526
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.27642247T>G
GRCh37
chr18:g.25222211T>G
Linked Data - Sequence & Population
gnomAD v2:
18:25222211 T / G
gnomAD v3:
18:27642247 T / G
gnomAD v4:
chr18-27642247-T-G
Joint Max Group AF
0.05912257 (MID)
Genomes Max Group AF
0.05514111 (NFE)
Linked Data - NCBI & NCI
dbSNP:
17665021
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.27642247T>G , CM000680.2:g.27642247T>G
GRCh38
NC_000018.9:g.25222211T>G , CM000680.1:g.25222211T>G
GRCh37
NC_000018.8:g.23476209T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'