ClinGen Allele Registry
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Canonical Allele Identifier:
CA14406858
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.56772968A>G
GRCh37
chr17:g.54850329A>G
Linked Data - Sequence & Population
gnomAD v2:
17:54850329 A / G
gnomAD v3:
17:56772968 A / G
gnomAD v4:
chr17-56772968-A-G
Joint Max Group AF
0.78626135 (EAS)
Genomes Max Group AF
0.78626135 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4794665
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.56772968A>G , CM000679.2:g.56772968A>G
GRCh38
NC_000017.10:g.54850329A>G , CM000679.1:g.54850329A>G
GRCh37
NC_000017.9:g.52205328A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'