ClinGen Allele Registry
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Canonical Allele Identifier:
CA298549969
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.34447199G>T
GRCh37
chr18:g.32027163G>T
Linked Data - Sequence & Population
gnomAD v2:
18:32027163 G / T
gnomAD v3:
18:34447199 G / T
gnomAD v4:
chr18-34447199-G-T
Joint Max Group AF
0.35973882 (AMR)
Genomes Max Group AF
0.35973882 (AMR)
Linked Data - NCBI & NCI
dbSNP:
1521791
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.34447199G>T , CM000680.2:g.34447199G>T
GRCh38
NC_000018.9:g.32027163G>T , CM000680.1:g.32027163G>T
GRCh37
NC_000018.8:g.30281161G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'