ClinGen Allele Registry
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Canonical Allele Identifier:
CA738051367
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.67307127C>G
GRCh37
chr1:g.67772810C>G
Linked Data - Sequence & Population
gnomAD v3:
1:67307127 C / G
gnomAD v4:
chr1-67307127-C-G
Joint Max Group AF
0.00000488 (NFE)
Genomes Max Group AF
0.00000488 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11810249
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.67307127C>G , CM000663.2:g.67307127C>G
GRCh38
NC_000001.10:g.67772810C>G , CM000663.1:g.67772810C>G
GRCh37
NC_000001.9:g.67545398C>G
NCBI36
NG_032977.1:g.4764C>G
NG_032977.2:g.4777C>G
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