ClinGen Allele Registry
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Canonical Allele Identifier:
CA223896276
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.64778919C>A
GRCh37
chr11:g.64546391C>A
Linked Data - Sequence & Population
gnomAD v4:
chr11-64778919-C-A
Linked Data - NCBI & NCI
dbSNP:
606458
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.64778919C>A , CM000673.2:g.64778919C>A
GRCh38
NC_000011.9:g.64546391C>A , CM000673.1:g.64546391C>A
GRCh37
NC_000011.8:g.64302967C>A
NCBI36
NG_021399.1:g.4926G>T , LRG_617:g.4926G>T
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