ClinGen Allele Registry
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Canonical Allele Identifier:
CA781034295
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.60373390A>G
GRCh37
chr18:g.58040623A>G
Linked Data - Sequence & Population
gnomAD v3:
18:60373390 A / G
gnomAD v4:
chr18-60373390-A-G
Linked Data - NCBI & NCI
dbSNP:
1224234953
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.60373390A>G , CM000680.2:g.60373390A>G
GRCh38
NC_000018.9:g.58040623A>G , CM000680.1:g.58040623A>G
GRCh37
NC_000018.8:g.56191603A>G
NCBI36
NG_016441.1:g.4379T>C
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