Canonical Allele Identifier: CA15976227
Gene:
MyVariant.info:
GRCh38 chr20:g.7125642T>C
GRCh37 chr20:g.7106289T>C
gnomAD v2:
20:7106289 T / C
gnomAD v3:
20:7125642 T / C
gnomAD v4:
chr20-7125642-T-C
Joint Max Group AF 0.58758134 (AFR)
Genomes Max Group AF 0.58758134 (AFR)
ClinVar RCV:
RCV000490626
ClinVar Variation:
427724
dbSNP:
1884302
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.7125642T>C , CM000682.2:g.7125642T>C GRCh38
NC_000020.10:g.7106289T>C , CM000682.1:g.7106289T>C GRCh37
NC_000020.9:g.7054289T>C NCBI36
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