ClinGen Allele Registry
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Canonical Allele Identifier:
CA297564757
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.25677222T>C
GRCh37
chr18:g.23257186T>C
Linked Data - Sequence & Population
gnomAD v2:
18:23257186 T / C
gnomAD v3:
18:25677222 T / C
gnomAD v4:
chr18-25677222-T-C
Joint Max Group AF
0.72847005 (SAS)
Genomes Max Group AF
0.72847005 (SAS)
Linked Data - NCBI & NCI
dbSNP:
1840440
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.25677222T>C , CM000680.2:g.25677222T>C
GRCh38
NC_000018.9:g.23257186T>C , CM000680.1:g.23257186T>C
GRCh37
NC_000018.8:g.21511184T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'