ClinGen Allele Registry
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Canonical Allele Identifier:
CA579790553
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.11765947C>G
GRCh37
chr8:g.11623456C>G
Linked Data - Sequence & Population
gnomAD v2:
8:11623456 C / G
gnomAD v3:
8:11765947 C / G
gnomAD v4:
chr8-11765947-C-G
Linked Data - NCBI & NCI
dbSNP:
1466785
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.11765947C>G , CM000670.2:g.11765947C>G
GRCh38
NC_000008.10:g.11623456C>G , CM000670.1:g.11623456C>G
GRCh37
NC_000008.9:g.11660865C>G
NCBI36
NG_053043.1:g.1285C>G
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