Canonical Allele Identifier: CA8070666
Gene:
MyVariant.info:
GRCh38 chr16:g.56960616C>T
GRCh37 chr16:g.56994528C>T
gnomAD v2:
16:56994528 C / T
gnomAD v3:
16:56960616 C / T
gnomAD v4:
chr16-56960616-C-T
Joint Max Group AF 0.33176416 (SAS)
Genomes Max Group AF 0.32228451 (SAS)
Exomes Max Group AF 0.33158783 (SAS)
dbSNP:
17231506
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56960616C>T , CM000678.2:g.56960616C>T GRCh38
NC_000016.9:g.56994528C>T , CM000678.1:g.56994528C>T GRCh37
NC_000016.8:g.55552029C>T NCBI36
NG_008952.1:g.3694C>T
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