ClinGen Allele Registry
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Canonical Allele Identifier:
CA301725411
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.62399655A>G
GRCh37
chr18:g.60066888A>G
Linked Data - Sequence & Population
gnomAD v3:
18:62399655 A / G
gnomAD v4:
chr18-62399655-A-G
Linked Data - NCBI & NCI
dbSNP:
2957137
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.62399655A>G , CM000680.2:g.62399655A>G
GRCh38
NC_000018.9:g.60066888A>G , CM000680.1:g.60066888A>G
GRCh37
NC_000018.8:g.58217868A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'