Canonical Allele Identifier: CA10818125
Gene:
MyVariant.info:
GRCh38 chr1:g.169586812C>T
GRCh37 chr1:g.169556050C>T
gnomAD v2:
1:169556050 C / T
gnomAD v3:
1:169586812 C / T
gnomAD v4:
chr1-169586812-C-T
Joint Max Group AF 0.63451744 (EAS)
Genomes Max Group AF 0.63451744 (EAS)
ClinVar RCV:
RCV001621208
ClinVar Variation:
1232860
dbSNP:
2269648
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586812C>T , CM000663.2:g.169586812C>T GRCh38
NC_000001.10:g.169556050C>T , CM000663.1:g.169556050C>T GRCh37
NC_000001.9:g.167822674C>T NCBI36
NG_011806.1:g.4720G>A , LRG_553:g.4720G>A
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