ClinGen Allele Registry
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Canonical Allele Identifier:
CA668632134
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.77641558T>A
GRCh37
chr10:g.79401316T>A
Linked Data - Sequence & Population
gnomAD v3:
10:77641558 T / A
gnomAD v4:
chr10-77641558-T-A
Joint Max Group AF
0.0000192 (AFR)
Genomes Max Group AF
0.0000192 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7071206
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.77641558T>A , CM000672.2:g.77641558T>A
GRCh38
NC_000010.10:g.79401316T>A , CM000672.1:g.79401316T>A
GRCh37
NC_000010.9:g.79071322T>A
NCBI36
NG_012270.1:g.1262A>T
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