ClinGen Allele Registry
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Canonical Allele Identifier:
CA14587965
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.59084822G>C
GRCh37
chr18:g.56752054G>C
Linked Data - Sequence & Population
gnomAD v2:
18:56752054 G / C
gnomAD v3:
18:59084822 G / C
gnomAD v4:
18:59084822 G / C
Linked Data - NCBI & NCI
dbSNP:
1037757
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.59084822G>C , CM000680.2:g.59084822G>C
GRCh38
NC_000018.9:g.56752054G>C , CM000680.1:g.56752054G>C
GRCh37
NC_000018.8:g.54903034G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'