ClinGen Allele Registry
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Canonical Allele Identifier:
CA732294678
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.22633861C>A
GRCh37
chr1:g.22960354C>A
Linked Data - Sequence & Population
gnomAD v3:
1:22633861 C / A
gnomAD v4:
chr1-22633861-C-A
Linked Data - NCBI & NCI
dbSNP:
665691
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.22633861C>A , CM000663.2:g.22633861C>A
GRCh38
NC_000001.10:g.22960354C>A , CM000663.1:g.22960354C>A
GRCh37
NC_000001.9:g.22832941C>A
NCBI36
NG_007282.1:g.2237C>A , LRG_22:g.2237C>A
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