ClinGen Allele Registry
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Canonical Allele Identifier:
CA295496911
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.2825420T>A
GRCh37
chr18:g.2825418T>A
Linked Data - Sequence & Population
gnomAD v2:
18:2825418 T / A
gnomAD v3:
18:2825420 T / A
gnomAD v4:
chr18-2825420-T-A
Joint Max Group AF
0.00016678 (AFR)
Genomes Max Group AF
0.00016678 (AFR)
Linked Data - NCBI & NCI
dbSNP:
673783
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.2825420T>A , CM000680.2:g.2825420T>A
GRCh38
NC_000018.9:g.2825418T>A , CM000680.1:g.2825418T>A
GRCh37
NC_000018.8:g.2815418T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'