ClinGen Allele Registry
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Canonical Allele Identifier:
CA36362730
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.200734413C>A
GRCh37
chr1:g.200703541C>A
Linked Data - Sequence & Population
gnomAD v3:
1:200734413 C / A
gnomAD v4:
chr1-200734413-C-A
Linked Data - NCBI & NCI
dbSNP:
6660197
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.200734413C>A , CM000663.2:g.200734413C>A
GRCh38
NC_000001.10:g.200703541C>A , CM000663.1:g.200703541C>A
GRCh37
NC_000001.9:g.198970164C>A
NCBI36
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