ClinGen Allele Registry
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Canonical Allele Identifier:
CA13291069
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr10:g.61589009G>T
GRCh37
chr10:g.63348767G>T
Linked Data - Sequence & Population
gnomAD v2:
10:63348767 G / T
gnomAD v3:
10:61589009 G / T
gnomAD v4:
chr10-61589009-G-T
Joint Max Group AF
0.67788384 (AFR)
Genomes Max Group AF
0.67788384 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1350172
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.61589009G>T , CM000672.2:g.61589009G>T
GRCh38
NC_000010.10:g.63348767G>T , CM000672.1:g.63348767G>T
GRCh37
NC_000010.9:g.63018773G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'