ClinGen Allele Registry
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Canonical Allele Identifier:
CA16393179
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.67875446T>A
GRCh37
chr10:g.69635204T>A
Linked Data - Sequence & Population
gnomAD v2:
10:69635204 T / A
gnomAD v3:
10:67875446 T / A
gnomAD v4:
chr10-67875446-T-A
Joint Max Group AF
0.28913039 (EAS)
Genomes Max Group AF
0.28913039 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10509291
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.67875446T>A , CM000672.2:g.67875446T>A
GRCh38
NC_000010.10:g.69635204T>A , CM000672.1:g.69635204T>A
GRCh37
NC_000010.9:g.69305210T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'