ClinGen Allele Registry
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Canonical Allele Identifier:
CA208448003
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.61147197T>A
GRCh37
chr10:g.62906955T>A
Linked Data - Sequence & Population
gnomAD v3:
10:61147197 T / A
gnomAD v4:
chr10-61147197-T-A
Joint Max Group AF
0.00000802 (AFR)
Genomes Max Group AF
0.00000802 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10761570
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.61147197T>A , CM000672.2:g.61147197T>A
GRCh38
NC_000010.10:g.62906955T>A , CM000672.1:g.62906955T>A
GRCh37
NC_000010.9:g.62576961T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'